Work

DNA Studies of Limb-Girdle Muscular Dystrophy Type 2A in the Amish Exclude a Modifying Mitochondrial Gene and Show No Evidence for a Modifying Nuclear Gene

Year: 1997

Type: article

Source: The American Journal of Human Genetics

DOI: 10.1016/s0002-9297(07)64296-7

Authors: V.M. Pratt, C.E. Jackson, D.C. Wallace, D.S. Gurley, A. Feit, G.L. Feldman

Institutions: Henry Ford Hospital, Emory University

Language: English

Topic: Muscle Physiology and Disorders

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: bronze

Funders: Muscular Dystrophy Association, National Institutes of Health, National Heart, Lung, and Blood Institute, National Institute of Neurological Disorders and Stroke

Awards: MITOCHONDRIAL GENES AND CARDIOVASCULAR DISEASES, G2718742063, G592126098, Mitochondrial Inborn Errors in Metabolism

OpenAlex ID: W1966755927

FWCI: 0.225

Cites: 7

Cited by: 4

Related to: 10