Work

Autosomal recessive hereditary neuropathy with focally folded myelin sheaths and linked to chromosome 11q23: a distinct and homogeneous entity

Year: 2000

Type: article

Study design: Case Report

Source: Neuromuscular Disorders

DOI: 10.1016/s0960-8966(99)00057-7

Authors: M.A.M Salih, T Maisonobe, M Kabiraj, M Al Rayess, M.H.S Al-Turaiki, M Akbar, A Tahan, J.A Urtizberea, D Grid, T Hamadouche, A Guilbot, A Brice, E Leguern

Institutions: King Saud University, King Khalid University Hospital, Pitié-Salpêtrière Hospital, Genethon (France), Inserm, Institut Pasteur d'Algérie

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: W2060123490

FWCI: 0.775

Cites: 23

Cited by: 20

Related to: 10