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A novel point mutation (D380A) and a rare deletion (1255deI55) in the glucocerebrosidase gene causing Gaucher's disease
Walley, Andrew J, Harris, AnnVolume:
2
Year:
1993
Language:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/2.10.1737
File:
PDF, 966 KB
english, 1993