## Abstract The g.ORF15 + 652–653delAG mutation in the __RPGR__ gene is the most frequent mutation in X‐linked retinitis pigmentosa (XLRP). The objective of this study was to investigate the possibility of mosaicism in an XLRP family. Eight subjects in the RP family were recruited. Blood samples we
✦ LIBER ✦
Linkage studies in X-linked retinitis pigmentosa
✍ Scribed by Gr�tzner, Peter ;Sanger, Ruth ;Spivey, Bruce E.
- Publisher
- Springer-Verlag
- Year
- 1972
- Weight
- 246 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0018-7348
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