Frequency and phenotype of patients carrying TPM2 and TPM3 gene mutations in a cohort of 94 patients with congenital myopathy
Citirak, Gülsenay, Witting, Nanna, Duno, Morten, Werlauff, Ulla, Petri, Helle, Vissing, JohnVolume:
24
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2013.12.008
Date:
April, 2014
File:
PDF, 1.23 MB
english, 2014