P412 Expanding the clinical and genetic spectrum of biallelic pathogenic MYO18B variants in congenital myopathy
Author:
S. Donkervoort,I. Zaharieva,M. Essid,C. Longman,A. Foley,I. Horrocks,H. Benrhouma,M. Farrugia,S. Neuhaus,T. Younes,I. Youssef-Turki,Y. Jamshidi,K. Chao,H. Houlden,R. Maroofian,C. Bönnemann,F. Muntoni,A. Sarkozy
Publication:
Neuromuscular Disorders
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