The wide spectrum of clinical manifestations resulting from glucocerebrosidase deficiency complicates genetic counseling for Gaucher disease. The identification of mutations in the glucocerebrosidase gene has enabled studies of genotype-phenotype correlation. However, a genotypic analysis of 60 type
β¦ LIBER β¦
DNA mutation analysis of Gaucher patients
β Scribed by Sidransky, Ellen ;Tsuji, Shoji ;Martin, Brian M. ;Stubblefield, Barbara ;Ginns, Edward I.
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 630 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0148-7299
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