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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
show all 9
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
show all 7
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