Gaucher disease mutations in non-Jewish patients
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1993.tb03185.x/fullpdf
Reference29 articles.
1. Assignment of the gene coding for human β-glucocerebrosidase to the region q21-q31 of chromosome 1 using monoclonal antibodies
2. Gaucher disease: new molecular approaches to diagnosis and treatment
3. Gaucher disease associated with a unique Kphl restriction site: identification of the amino-acid substitution
4. Identification of the second common Jewish Gaucher disease mutation makes possible population-based screening for the heterozygous state.
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