Work

Congenital hypomyelination due to myelin protein zero Q215X mutation

Year: 1999

Type: article

Study design: Case Report

Source: Annals of Neurology

DOI: 10.1002/1531-8249(199905)45:5<676::aid-ana21>3.0.co;2-k

Authors: P. Mandich, G. L. Mancardi, A. Varese, S. Soriani, E. Di Maria, E. Bellone, M. Bado, L. Gross, A. J. Windebank, F. Ajmar, A. Schenone

Institutions: Istituto Giannina Gaslini, University of Genoa, Mayo Clinic

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: W2012242545

FWCI: 1.403

Cites: 17

Cited by: 57

Related to: 10