Gaucher disease is the most prevalent lysosomal storage disease. It is panethnic and results from an inherited deficiency of glucocerebrosidase. Most mutations to date have been identified among Jewish and non-Jewish Caucasian patients; mutations in Chinese patients are largely unknown. We have perf
โฆ LIBER โฆ
Mutation prevalence among 47 unrelated Japanese patients with Gaucher disease: identification of four novel mutations
โ Scribed by H. Ida; O. M. Rennert; H. Kawame; K. Maekawa; Y. Eto
- Book ID
- 110222658
- Publisher
- Springer
- Year
- 1997
- Tongue
- English
- Weight
- 308 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0141-8955
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