Work

Clinical, electrophysiologic, and molecular correlations in 13 families with hereditary neuropathy with liability to pressure palsies and a chromosome 17p11.2 deletion

Year: 1995

Type: article

Study design: Observational Study

Source: Neurology

DOI: 10.1212/wnl.45.11.2018

Authors: R. Gouider, E. LeGuern, M. Gugenheim, S. Tardieu, T. Maisonobe, J. M. Léger, J. M. Vallat, Y. Agid, P. Bouche, A. Brice

Institutions: Inserm, Physiopathologie des Comportements

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: W1979526330

FWCI: 1.733

Cites:

Cited by: 109

Related to: 10