High Frequency of GBA Gene Mutations in Dementia With Lewy Bodies Among Ashkenazi Jews
Author(s) -
Tamara Shiner,
Anat Mirelman,
Mali Gana Weisz,
Anat BarShira,
Elissa L. Ash,
Ron Cialic,
Naomi Nevler,
Tanya Gurevich,
Noa Bregman,
Avi OrrUrtreger,
Nir Giladi
Publication year - 2016
Publication title -
jama neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.298
H-Index - 231
eISSN - 2168-6157
pISSN - 2168-6149
DOI - 10.1001/jamaneurol.2016.1593
Subject(s) - dementia with lewy bodies , rem sleep behavior disorder , dementia , medicine , lewy body , gene mutation , psychology , psychiatry , disease , pediatrics , parkinson's disease , mutation , genetics , biology , gene
Mutations in the glucocerebrosidase (GBA) gene are a risk factor for the development of dementia with Lewy bodies (DLB). These mutations are common among Ashkenazi Jews (AJ) and appear to have an effect on the natural history of the disease.
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