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

✍ Scribed by Gerber, Sylvie; Perrault, Isabelle; Hanein, Sylvain; Barbet, Fabienne; Ducroq, Dominique; Ghazi, Imad; Martin-Coignard, Dominique; Leowski, Corinne; Homfray, Tessa; Dufier, Jean-Louis

• Book ID: 110025166
• Publisher: Nature Publishing Group
• Year: 2001
• Tongue: English
• Weight: 533 KB
• Volume: 9
• Category: Article
• ISSN: 1018-4813
• DOI: 10.1038/sj.ejhg.5200689