A start codon CMT1X mutation associated with transient encephalomyelitis causes complete loss of Cx32

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Authors: Irene Sargiannidou, Gun-Ha Kim, Styliana Kyriakoudi, Baik-Lin Eun, Kleopas A. Kleopa

Journal title: neurogenetics

Journal number: 13646745

Journal publisher: Springer Verlag

Published year: 2015

Published pages: 193-200

DOI identifier: 10.1007/s10048-015-0442-4

ISSN: 1364-6745