TY  - GEN
AU  - Perrault,Isabelle
AU  - Estrada-Cuzcano,Alejandro
AU  - Lopez,Irma
AU  - Kohl,Susanne
AU  - Li,Shiqiang
AU  - Testa,Francesco
AU  - Zekveld-Vroon,Renate
AU  - Wang,Xia
AU  - Pomares,Esther
AU  - Andorf,Jean
AU  - Aboussair,Nisrine
AU  - Banfi,Sandro
AU  - Delphin,Nathalie
AU  - den Hollander,Anneke I
AU  - Edelson,Catherine
AU  - Florijn,Ralph
AU  - Jean-Pierre,Marc
AU  - Leowski,Corinne
AU  - Megarbane,Andre
AU  - Villanueva,Cristina
AU  - Flores,Blanca
AU  - Munnich,Arnold
AU  - Ren,Huanan
AU  - Zobor,Ditta
AU  - Bergen,Arthur
AU  - Chen,Rui
AU  - Cremers,Frans P M
AU  - Gonzalez-Duarte,Roser
AU  - Koenekoop,Robert K
AU  - Simonelli,Francesca
AU  - Stone,Edwin
AU  - Wissinger,Bernd
AU  - Zhang,Qingjiong
AU  - Kaplan,Josseline
AU  - Rozet,Jean-Michel
TI  - Union makes strength: a worldwide collaborative genetic and clinical study to provide a comprehensive survey of RD3 mutations and delineate the associated phenotype
SN  - 1932-6203
PY  - 2013///0701
KW  - Adolescent
KW  - Adult
KW  - Canada
KW  - Child
KW  - Child, Preschool
KW  - China
KW  - Cohort Studies
KW  - Europe
KW  - Eye Proteins
KW  - genetics
KW  - Female
KW  - Humans
KW  - Infant
KW  - Leber Congenital Amaurosis
KW  - Linkage Disequilibrium
KW  - Male
KW  - Mutation
KW  - Pedigree
KW  - Phenotype
KW  - Polymorphism, Genetic
KW  - Retina
KW  - metabolism
KW  - Retinal Degeneration
KW  - United States
KW  - Young Adult
N1  - Publication Type: Journal Article; Multicenter Study; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1371/journal.pone.0051622
ER  -