Work

Homozygosity mapping of an autosomal recessive form of demyelinating Charcot-Marie-Tooth disease to chromosome 5q23-q33

Year: 1997

Type: article

Study design: Observational Study

Source: Neuromuscular Disorders

DOI: 10.1016/s0960-8966(97)87322-1

Authors: E. LeGuern, A. Guilbot, M. Kessali, N. Ravise, J. Tassin, T. Maisonobe, D. Grid, A. Brice

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

OpenAlex ID: W2017828736

FWCI: 0.65

Cites:

Cited by: 12

Related to: 10