Communicated by William S. Sly Gaucher disease is the most prevalent sphingolipidosis, characterized by genetic deficiency of lysosomal hydrolase glucocerebrosidase, and is inherited in an autosomal recessive manner. To characterize the molecular basis of Gaucher disease in Japan, we analyzed for th
β¦ LIBER β¦
Molecular analysis of gaucher disease: Screening of patients in the Montreal/Quebec region
β Scribed by Choy, Francis Y. M. ;Woo, Mary ;Der Kaloustian, Vazken M.
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 635 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0148-7299
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