Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosis.

Sylvie Gerber,Isabelle Perrault,Sylvain Hanein,Fabienne Barbet,Dominique Ducroq,Imad Ghazi,Dominique Martin-Coignard,Corinne Leowski,Tessa Homfray,Jean Louis Dufier,Arnold Munnich,Josseline Kaplan,Jean-Michel Rozet

Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosis.

2001

Sylvie Gerber
Isabelle Perrault
Sylvain Hanein
Fabienne Barbet
Dominique Ducroq
Imad Ghazi
Dominique Martin-Coignard
Corinne Leowski
Tessa Homfray
Jean Louis Dufier
Arnold Munnich
Josseline Kaplan
Jean-Michel Rozet

Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosis

Keywords:

Biology
Leber congenital amaurosis
Genetics
CRB1
RPGR-INTERACTING PROTEIN
Retinitis pigmentosa GTPase regulator
Exon
Bioinformatics
Intron
Gene
RPGRIP1 gene
Genome
Chromosome

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