Gaucher Disease Type 1: Cloning and Characterization of a cDNA Encoding Acid β-Glucosidase from an Ashkenazi Jewish Patient
Author:
Publisher
Mary Ann Liebert Inc
Subject
Genetics,Molecular Biology,Biochemistry
Link
http://www.liebertpub.com/doi/pdf/10.1089/dna.1.1988.7.521
Reference18 articles.
1. Glucocerebrosidase processing in normal fibroblasts and in fibroblasts from patients with type I, type II, and type III Gaucher disease.
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4. Detection of sickle cell beta S-globin allele by hybridization with synthetic oligonucleotides.
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