Work

Gaucher disease type 2 — Homozygosity for the mutation F331S in two unrelated consanguineous Muslim Arab patients with Gaucher disease from the Gaza and Jenin regions

Year: 2011

Type: article

Study design: Case Report

Source: Blood Cells Molecules and Diseases

DOI: 10.1016/j.bcmd.2011.08.002

Authors: Hagit N. Baris, Annick Raas-Rothschild, Ben-Zion Garty, Ruth Tor, Sarah Klontz, Nahid Tayebi, Ellen Sidransky, Ian J. Cohen

Institutions: Tel Aviv University, Rabin Medical Center, Hadassah Medical Center, Schneider Children's 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

Award: Genetic and clinical studies of Gaucher disease and other lysosomal disorders

OpenAlex ID: W2078175475

FWCI:

Cites: 9

Cited by:

Related to: 10