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Different Functional Outcome of RetGC1 and RPE65 Gene Mutations in Leber Congenital Amaurosis
Different Functional Outcome of RetGC1 and RPE65 Gene Mutations in Leber Congenital Amaurosis
1999
Isabelle Perrault
Jean-Michel Rozet
Imad Ghazi
Corinne Leowski
Michèle Bonnemaison
Sylvie Gerber
Dominique Ducroq
Annick Cabot
Eric Souied
Jean Louis Dufier
Arnold Munnich
Josseline Kaplan
Keywords:
Consanguinity
CRB1
Leber congenital amaurosis
Genetics
Phenotype
RPE65
Mutation
Gene
Genetic linkage
Biology
Blindness
gene mutation
Correction
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