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

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Year: 2009
Type: article
Source: Blood Cells Molecules and Diseases
DOI: 10.1016/j.bcmd.2009.08.004
Authors: Shraga Aviner, Ben-Zion Garty, Avinoam Rachmel, Hagit N. Baris, Ellen Sidransky, Avinoam Shuffer, Joseph Attias, Yisaac Yaniv, Ian J. Cohen
Institutions: Ben-Gurion University of the Negev, Barzilai Medical Center, Tel Aviv University, Schneider Children's Medical Center, Rabin Medical Center, National Institutes of Health, National Human Genome Research Institute
Language: English

Topic: Lysosomal Storage Disorders Research
Subfield: Physiology
Field: Medicine
Domain: Health Sciences
SDG: Good health and well-being

Open Access status: green

Funders: National Institutes of Health, National Human Genome Research Institute
Awards: "Genetic and clinical studies of Gaucher disease and other lysosomal disorders", Genetic and clinical studies of Gaucher disease and other lysosomal disorders
OpenAlex ID: W2029938281
FWCI: 1.105
Cites: 22
Cited by: 20
Related to: 10
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