Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosis. (Q34088707)
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scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosis. |
scientific article |
Statements
Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosis (English)
Hanein S
Barbet F
Ducroq D
Ghazi I
Martin-Coignard D
Leowski C
Homfray T
Dufier JL
Kaplan J
1 August 2001