## How Fancbni anemia (FA) is a rare autosomal recessive disease characterized by diverse clinical symptoms, chromosomal instability, and hypersensitivity
First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy
β Scribed by Dr. G. Christoph Korenke; Ernst Krasemann; Volker Meier; Wolfgang Beuche; D.H. Hunneman; F. Hanefeld
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 272 KB
- Volume
- 11
- Category
- Article
- ISSN
- 1059-7794
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