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Gaucher disease: the origins of the Ashkenazi Jewish N370S and 84GG acid beta-glucosidase mutations.
Diaz, G A; Gelb, B D; Risch, N; Nygaard, T G; Frisch, A; Cohen, I J; Miranda, C S; Amaral, O; Maire, I; Poenaru, L; Caillaud, C; Weizberg, M; Mistry, P; Desnick, R J.
Affiliation
  • Diaz GA; Department of Human Genetics, Mount Sinai School of Medicine, New York, NY 10029, USA.
Am J Hum Genet ; 66(6): 1821-32, 2000 Jun.
Article in En | MEDLINE | ID: mdl-10777718
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Jews / Founder Effect / Mutation, Missense / Gaucher Disease / Glucosylceramidase Type of study: Prognostic_studies Limits: Humans Country/Region as subject: Europa Language: En Journal: Am J Hum Genet Year: 2000 Document type: Article Affiliation country: United States
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Jews / Founder Effect / Mutation, Missense / Gaucher Disease / Glucosylceramidase Type of study: Prognostic_studies Limits: Humans Country/Region as subject: Europa Language: En Journal: Am J Hum Genet Year: 2000 Document type: Article Affiliation country: United States