The clinical importance of sequence variations in the ABCA4 gene has been extensively discussed during the last decade. Mutations in the ABCA4 gene are involved in several forms of inherited retinal degenerations. We screened all 50 exons of the ABCA4 gene in a cohort of 5 Stargardt Disease (STGD) a
✦ LIBER ✦
Stargardt's disease and retinitis pigmentosa: different phenotypic presentations in the same family
✍ Scribed by Özdek, Ş; Onaran, Z; Gürelik, G; Bilgihan, K; Acar, C; Hasanreiso[gcaron]lu, B
- Book ID
- 110035815
- Publisher
- Nature Publishing Group
- Year
- 2005
- Tongue
- English
- Weight
- 211 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0950-222X
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