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Novel familial pathogenic mutation in gap junction protein, beta‐1 gene ( GJB1 ) associated with transient neurological deficits in a patient with X‐linked Charcot‐Marie‐Tooth disease
Author(s) -
Appu Merveen,
Mar Soe
Publication year - 2014
Publication title -
muscle and nerve
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.025
H-Index - 145
eISSN - 1097-4598
pISSN - 0148-639X
DOI - 10.1002/mus.24343
Subject(s) - neurology , pediatric neurology , clinical neurology , medicine , psychology , pediatrics , neuroscience , psychiatry