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Type 2 Gaucher disease occurs in Ashkenazi Jews but is surprisingly rare

  • Published:2009-11 Issue:3 Volume:43 Page:294-297
  • ISSN:1079-9796
  • Container-title:Blood Cells, Molecules, and Diseases
  • language:en
  • Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Aviner Shraga,Garty Ben-Zion,Rachmel Avinoam,Baris Hagit N.,Sidransky Ellen,Shuffer Avinoam,Attias Joseph,Yaniv Yisaac,Cohen Ian J.

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference21 articles.

1. Genetics of the sphingolipidoses;Knudson,1962

2. Glucosyl ceramid lipidoses: Gaucher's disease;Frederickson,1972

3. Gaucher disease-Norrbottnian type: Neurodevelopmental, neurological and neuropsychological aspects;Bloom;Eur. J. Pediatr.,1983

4. Gaucher disease in the neonate: a distinct Gaucher phenotype is analogous to a mouse model created by targeted disruption of the glucocerebrosidase gene;Sidransky;Pediatr. Res.,1992

5. Glucosylceramid lipidoses: Gaucher disease;Beutler,1995

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