β-galactosidase deficiency: Prolonged survival in three patients following early central nervous system deterioration
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1978.tb01185.x/fullpdf
Reference12 articles.
1. Genetic heterogeneity in GM1 gangliosidosis;Galjaard;Nature (Lond.),1975
2. Macular cherry-red spot, corneal clouding, and β-galactosidase deficiency;Goldberg;Arch, intern. Med.,1971
3. β-galactosidase deficiency in an adult: A biochemical and somatic cell genetic study on a variant of GM1 gangliosidosis;Koster;Clin. Gen.,1976
4. Juvenile GM1 gangliosidosis;Lowden;Arch Neurol. (Chic.),1974
5. Molecular genetics of GM1β-galactosidase;O'Brien;Clin. Genet.,1975
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