Mutations in the RP2 gene cause disease in 10% of families with familial X-linked retinitis pigmentosa assessed in this study

Hardcastle, AJ Thiselton, DL Van Maldergem, L Saha, BK Jay, M Plant, C Taylor, R Bird, AC Bhattacharya, S

Aj. Hardcastle et al., Mutations in the RP2 gene cause disease in 10% of families with familial X-linked retinitis pigmentosa assessed in this study, AM J HU GEN, 64(4), 1999, pp. 1210-1215

15

Research/Laboratory Medicine & Medical Tecnology","Molecular Biology & Genetics

AMERICAN JOURNAL OF HUMAN GENETICS

00029297 → ACNP

64

4

1999

1210 - 1215

ISI

0002-9297(199904)64:4<1210:MITRGC>2.0.ZU;2-L