Original language | English (US) |
---|---|
Pages (from-to) | 1109 |
Number of pages | 1 |
Journal | European Journal of Human Genetics |
Volume | 19 |
Issue number | 10 |
DOIs |
|
State | Published - Oct 2011 |
Externally published | Yes |
ASJC Scopus subject areas
- Genetics
- Genetics(clinical)
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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.; Kenna, Paul F.; Tam, Lawrence C.S.; Kiang, Anna S.; Campbell, Matthew; Weinstock, George M.; Koboldt, Daniel C.; Ding, Li; Fulton, Robert S.; Sodergren, Erica J.; Allman, Denis; Millington-Ward, Sophia; Palfi, Arpad; McKee, Alex; Blanton, Susan H.; Slifer, Susan; Konidari, Ioanna; Farrar, G. Jane; Daiger, Stephen P.; Humphries, Peter.
In: European Journal of Human Genetics, Vol. 19, No. 10, 10.2011, p. 1109.Research output: Contribution to journal › Comment/debate › peer-review
}
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
N1 - Copyright: Copyright 2012 Elsevier B.V., All rights reserved.
PY - 2011/10
Y1 - 2011/10
UR - http://www.scopus.com/inward/record.url?scp=80053072511&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=80053072511&partnerID=8YFLogxK
U2 - 10.1038/ejhg.2011.132
DO - 10.1038/ejhg.2011.132
M3 - Comment/debate
AN - SCOPUS:80053072511
VL - 19
SP - 1109
JO - European Journal of Human Genetics
JF - European Journal of Human Genetics
SN - 1018-4813
IS - 10
ER -