Erratum: A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement (European Journal of Human Genetics (2011) 19 (1074-1081) DOI: 10.1038/ejhg.2011.86)

Sara J. Bowne; Marian M. Humphries; Lori S. Sullivan; Paul F. Kenna; Lawrence C.S. Tam; Anna S. Kiang; Matthew Campbell; George M. Weinstock; Daniel C. Koboldt; Li Ding; Robert S. Fulton; Erica J. Sodergren; Denis Allman; Sophia Millington-Ward; Arpad Palfi; Alex McKee; Susan H. Blanton; Susan Slifer; Ioanna Konidari; G. Jane Farrar; Stephen P. Daiger; Peter Humphries

doi:10.1038/ejhg.2011.132

Erratum: A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement (European Journal of Human Genetics (2011) 19 (1074-1081) DOI: 10.1038/ejhg.2011.86)

Sara J. Bowne, Marian M. Humphries, Lori S. Sullivan, Paul F. Kenna, Lawrence C.S. Tam, Anna S. Kiang, Matthew Campbell, George M. Weinstock, Daniel C. Koboldt, Li Ding, Robert S. Fulton, Erica J. Sodergren, Denis Allman, Sophia Millington-Ward, Arpad Palfi, Alex McKee, Susan H. Blanton, Susan Slifer, Ioanna Konidari, G. Jane FarrarStephen P. Daiger, Peter Humphries

Research output: Contribution to journal › Comment/debate

1 Scopus citations

Original language	English
Pages (from-to)	1109
Number of pages	1
Journal	European Journal of Human Genetics
Volume	19
Issue number	10
DOIs	https://doi.org/10.1038/ejhg.2011.132
State	Published - Oct 2011

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10.1038/ejhg.2011.132

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Bowne, S. J., Humphries, M. M., Sullivan, L. S., Kenna, P. F., Tam, L. C. S., Kiang, A. S., Campbell, M., Weinstock, G. M., Koboldt, D. C., Ding, L., Fulton, R. S., Sodergren, E. J., Allman, D., Millington-Ward, S., Palfi, A., McKee, A., Blanton, S. H., Slifer, S., Konidari, I., ... Humphries, P. (2011). Erratum: A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement (European Journal of Human Genetics (2011) 19 (1074-1081) DOI: 10.1038/ejhg.2011.86). European Journal of Human Genetics, 19(10), 1109. https://doi.org/10.1038/ejhg.2011.132

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title = "Erratum: A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement (European Journal of Human Genetics (2011) 19 (1074-1081) DOI: 10.1038/ejhg.2011.86)",

author = "Bowne, {Sara J.} and Humphries, {Marian M.} and Sullivan, {Lori S.} and Kenna, {Paul F.} and Tam, {Lawrence C.S.} and Kiang, {Anna S.} and Matthew Campbell and Weinstock, {George M.} and Koboldt, {Daniel C.} and Li Ding and Fulton, {Robert S.} and Sodergren, {Erica J.} and Denis Allman and Sophia Millington-Ward and Arpad Palfi and Alex McKee and Blanton, {Susan H.} and Susan Slifer and Ioanna Konidari and Farrar, {G. Jane} and Daiger, {Stephen P.} and Peter Humphries",

year = "2011",

month = oct,

doi = "10.1038/ejhg.2011.132",

language = "English",

volume = "19",

pages = "1109",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

number = "10",

}

Bowne, SJ, Humphries, MM, Sullivan, LS, Kenna, PF, Tam, LCS, Kiang, AS, Campbell, M, Weinstock, GM, Koboldt, DC, Ding, L , Fulton, RS, Sodergren, EJ, Allman, D, Millington-Ward, S, Palfi, A, McKee, A, Blanton, SH, Slifer, S, Konidari, I, Farrar, GJ, Daiger, SP & Humphries, P 2011, 'Erratum: A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement (European Journal of Human Genetics (2011) 19 (1074-1081) DOI: 10.1038/ejhg.2011.86)', European Journal of Human Genetics, vol. 19, no. 10, pp. 1109. https://doi.org/10.1038/ejhg.2011.132

Erratum: A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement (European Journal of Human Genetics (2011) 19 (1074-1081) DOI: 10.1038/ejhg.2011.86). / Bowne, Sara J.; Humphries, Marian M.; Sullivan, Lori S. et al.
In: European Journal of Human Genetics, Vol. 19, No. 10, 10.2011, p. 1109.

Research output: Contribution to journal › Comment/debate

TY - JOUR

T1 - Erratum

T2 - A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement (European Journal of Human Genetics (2011) 19 (1074-1081) DOI: 10.1038/ejhg.2011.86)

AU - Bowne, Sara J.

AU - Humphries, Marian M.

AU - Sullivan, Lori S.

AU - Kenna, Paul F.

AU - Tam, Lawrence C.S.

AU - Kiang, Anna S.

AU - Campbell, Matthew

AU - Weinstock, George M.

AU - Koboldt, Daniel C.

AU - Ding, Li

AU - Fulton, Robert S.

AU - Sodergren, Erica J.

AU - Allman, Denis

AU - Millington-Ward, Sophia

AU - Palfi, Arpad

AU - McKee, Alex

AU - Blanton, Susan H.

AU - Slifer, Susan

AU - Konidari, Ioanna

AU - Farrar, G. Jane

AU - Daiger, Stephen P.

AU - Humphries, Peter

PY - 2011/10

Y1 - 2011/10

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U2 - 10.1038/ejhg.2011.132

DO - 10.1038/ejhg.2011.132

M3 - Comment/debate

AN - SCOPUS:80053072511

SN - 1018-4813

VL - 19

SP - 1109

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - 10

ER -

Bowne SJ, Humphries MM, Sullivan LS, Kenna PF, Tam LCS, Kiang AS et al. Erratum: A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement (European Journal of Human Genetics (2011) 19 (1074-1081) DOI: 10.1038/ejhg.2011.86). European Journal of Human Genetics. 2011 Oct;19(10):1109. doi: 10.1038/ejhg.2011.132

Erratum: A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement (European Journal of Human Genetics (2011) 19 (1074-1081) DOI: 10.1038/ejhg.2011.86)

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