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Physical and Genetic Mapping of the CMT4A Locus and Exclusion of PMP-2 as the Defect in CMT4A

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Year: 1995
Type: article
Source: Genomics
DOI: 10.1006/geno.1995.1143
Authors: K.Ben Othmane, D. Loeb, R. Hayworth-Hodgte, F. Hentati, N. Rao, A.D. Roses, M.Ben Hamida, M.A. Pericak-Vance, J.M. Vance
Institutions: Atrium Health Wake Forest Baptist, Duke Medical Center, National Institute of Neurology Mongi-Ben Hamida, Duke University
Language: English

Topic: Hereditary Neurological Disorders
Subfield: Cellular and Molecular Neuroscience
Field: Neuroscience
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed

Funders: National Institutes of Health, National Institute of Neurological Disorders and Stroke
Awards: Genetic Studies in Neurological Disorders, CMT DISEASE--LOCALIZATION AND CLASSIFICATION OF TYPE 2, G939203996
OpenAlex ID: W2082706367
FWCI: 1.067
Cites:
Cited by: 27
Related to: 10
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