Mutations in the RP2 gene cause disease in 10% of families with familial X-linked retinitis pigmentosa assessed in this study (Q24540229)
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English | Mutations in the RP2 gene cause disease in 10% of families with familial X-linked retinitis pigmentosa assessed in this study |
scientific article |
Statements
Mutations in the RP2 gene cause disease in 10% of families with familial X-linked retinitis pigmentosa assessed in this study (English)
D L Thiselton
L Van Maldergem
B K Saha
M Jay
C Plant
R Taylor
A C Bird
S Bhattacharya