## Communicated by Albert de la Chapelle Choroideremia (CHM) is an X-linked recessive eye disease that results from mutations involving the Rab escort protein-1 (REP-1) gene. In 18 patients deletions of different sizes have been found. Two females suffering from CHM were reported to have transloca
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REP-1gene mutations in Japanese patients with choroideremia
โ Scribed by K. Fujiki; Yoshihiro Hotta; Mutsuko Hayakawa; Akio Saito; Yukihiko Mashima; Mikiro Mori; Masaru Yoshii; Akira Murakami; Masayuki Matsumoto; Seiji Hayasaka; Nobuko Tagami; Yasushi Isashiki; Norio Ohba; Atsushi Kanai
- Publisher
- Springer-Verlag
- Year
- 1999
- Tongue
- English
- Weight
- 272 KB
- Volume
- 237
- Category
- Article
- ISSN
- 0065-6100
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