Erratum: Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency (American Journal of Human Genetics (2011) 89 (28-43))

Alan F. Rope; Kai Wang; Rune Evjenth; Jinchuan Xing; Jennifer J. Johnston; Jeffrey J. Swensen; W. Evan Johnson; Barry Moore; Chad D. Huff; Lynne M. Bird; John C. Carey; John M. Opitz; Cathy A. Stevens; Tao Jiang; Christa Schank; Heidi Deborah Fain; Reid Robison; Brian Dalley; Steven Chin; Sarah T. South; Theodore J. Pysher; Lynn B. Jorde; Hakon Hakonarson; Johan R. Lillehaug; Leslie G. Biesecker; Mark Yandell; Thomas Arnesen; Gholson J. Lyon

doi:10.1016/j.ajhg.2011.07.008

Erratum: Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency (American Journal of Human Genetics (2011) 89 (28-43))

Alan F. Rope, Kai Wang, Rune Evjenth, Jinchuan Xing, Jennifer J. Johnston, Jeffrey J. Swensen, W. Evan Johnson, Barry Moore, Chad D. Huff, Lynne M. Bird, John C. Carey, John M. Opitz, Cathy A. Stevens, Tao Jiang, Christa Schank, Heidi Deborah Fain, Reid Robison, Brian Dalley, Steven Chin, Sarah T. SouthTheodore J. Pysher, Lynn B. Jorde, Hakon Hakonarson, Johan R. Lillehaug, Leslie G. Biesecker, Mark Yandell, Thomas Arnesen, Gholson J. Lyon

Research output: Contribution to journal › Comment/debate › peer-review

4 Scopus citations

Original language	English (US)
Pages (from-to)	345
Number of pages	1
Journal	American Journal of Human Genetics
Volume	89
Issue number	2
DOIs	https://doi.org/10.1016/j.ajhg.2011.07.008
State	Published - Aug 12 2011
Externally published	Yes

All Science Journal Classification (ASJC) codes

Genetics
Genetics(clinical)

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Rope, A. F., Wang, K., Evjenth, R., Xing, J., Johnston, J. J., Swensen, J. J., Johnson, W. E., Moore, B., Huff, C. D., Bird, L. M., Carey, J. C., Opitz, J. M., Stevens, C. A., Jiang, T., Schank, C., Fain, H. D., Robison, R., Dalley, B., Chin, S., ... Lyon, G. J. (2011). Erratum: Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency (American Journal of Human Genetics (2011) 89 (28-43)). American Journal of Human Genetics, 89(2), 345. https://doi.org/10.1016/j.ajhg.2011.07.008

Rope, Alan F. ; Wang, Kai ; Evjenth, Rune ; Xing, Jinchuan ; Johnston, Jennifer J. ; Swensen, Jeffrey J. ; Johnson, W. Evan ; Moore, Barry ; Huff, Chad D. ; Bird, Lynne M. ; Carey, John C. ; Opitz, John M. ; Stevens, Cathy A. ; Jiang, Tao ; Schank, Christa ; Fain, Heidi Deborah ; Robison, Reid ; Dalley, Brian ; Chin, Steven ; South, Sarah T. ; Pysher, Theodore J. ; Jorde, Lynn B. ; Hakonarson, Hakon ; Lillehaug, Johan R. ; Biesecker, Leslie G. ; Yandell, Mark ; Arnesen, Thomas ; Lyon, Gholson J. / Erratum : Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency (American Journal of Human Genetics (2011) 89 (28-43)). In: American Journal of Human Genetics. 2011 ; Vol. 89, No. 2. pp. 345.

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title = "Erratum: Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency (American Journal of Human Genetics (2011) 89 (28-43))",

author = "Rope, {Alan F.} and Kai Wang and Rune Evjenth and Jinchuan Xing and Johnston, {Jennifer J.} and Swensen, {Jeffrey J.} and Johnson, {W. Evan} and Barry Moore and Huff, {Chad D.} and Bird, {Lynne M.} and Carey, {John C.} and Opitz, {John M.} and Stevens, {Cathy A.} and Tao Jiang and Christa Schank and Fain, {Heidi Deborah} and Reid Robison and Brian Dalley and Steven Chin and South, {Sarah T.} and Pysher, {Theodore J.} and Jorde, {Lynn B.} and Hakon Hakonarson and Lillehaug, {Johan R.} and Biesecker, {Leslie G.} and Mark Yandell and Thomas Arnesen and Lyon, {Gholson J.}",

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Rope, AF, Wang, K, Evjenth, R, Xing, J, Johnston, JJ, Swensen, JJ, Johnson, WE, Moore, B, Huff, CD, Bird, LM, Carey, JC, Opitz, JM, Stevens, CA, Jiang, T, Schank, C, Fain, HD, Robison, R, Dalley, B, Chin, S, South, ST, Pysher, TJ, Jorde, LB, Hakonarson, H, Lillehaug, JR, Biesecker, LG, Yandell, M, Arnesen, T & Lyon, GJ 2011, 'Erratum: Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency (American Journal of Human Genetics (2011) 89 (28-43))', American Journal of Human Genetics, vol. 89, no. 2, pp. 345. https://doi.org/10.1016/j.ajhg.2011.07.008

Erratum : Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency (American Journal of Human Genetics (2011) 89 (28-43)). / Rope, Alan F.; Wang, Kai; Evjenth, Rune; Xing, Jinchuan; Johnston, Jennifer J.; Swensen, Jeffrey J.; Johnson, W. Evan; Moore, Barry; Huff, Chad D.; Bird, Lynne M.; Carey, John C.; Opitz, John M.; Stevens, Cathy A.; Jiang, Tao; Schank, Christa; Fain, Heidi Deborah; Robison, Reid; Dalley, Brian; Chin, Steven; South, Sarah T.; Pysher, Theodore J.; Jorde, Lynn B.; Hakonarson, Hakon; Lillehaug, Johan R.; Biesecker, Leslie G.; Yandell, Mark; Arnesen, Thomas; Lyon, Gholson J.

In: American Journal of Human Genetics, Vol. 89, No. 2, 12.08.2011, p. 345.

Research output: Contribution to journal › Comment/debate › peer-review

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AU - Rope, Alan F.

AU - Wang, Kai

AU - Evjenth, Rune

AU - Xing, Jinchuan

AU - Johnston, Jennifer J.

AU - Swensen, Jeffrey J.

AU - Johnson, W. Evan

AU - Moore, Barry

AU - Huff, Chad D.

AU - Bird, Lynne M.

AU - Carey, John C.

AU - Opitz, John M.

AU - Stevens, Cathy A.

AU - Jiang, Tao

AU - Schank, Christa

AU - Fain, Heidi Deborah

AU - Robison, Reid

AU - Dalley, Brian

AU - Chin, Steven

AU - South, Sarah T.

AU - Pysher, Theodore J.

AU - Jorde, Lynn B.

AU - Hakonarson, Hakon

AU - Lillehaug, Johan R.

AU - Biesecker, Leslie G.

AU - Yandell, Mark

AU - Arnesen, Thomas

AU - Lyon, Gholson J.

PY - 2011/8/12

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DO - 10.1016/j.ajhg.2011.07.008

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VL - 89

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JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

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ER -

Erratum: Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency (American Journal of Human Genetics (2011) 89 (28-43))

All Science Journal Classification (ASJC) codes

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