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 Farrar

Stephen 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

@article{4ee164e62e0440b6a63df837a4e7f3f5,

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

UR - https://www.scopus.com/pages/publications/80053072511

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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