Homozygosity for two mild glucocerebrosidase mutations of probable Iberian origin
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.1999.560117.x/fullpdf
Reference12 articles.
1. Use of denaturing gradient gel electrophoresis to identify mutant sequences in the β-glucocerebrosidase gene;Laubscher;Hum Mutat,1994
2. Type 1 Gaucher disease: identification of N396T and prevalence of glucocerebrosidase mutations in the Portuguese;Amaral;Hum Mutat,1996
3. Identification of Gaucher disease carriers: glucocerebrosidase antigen and DNA analysis;Lacerda;Biochem Med Metab Biol,1993
4. Comparative study on glucocerebrosidase in spleens from patients with Gaucher disease;Aerts;Biochem J,1990
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