Novel autosomal dominant TNNT1 mutation causing nemaline myopathy
Konersman, Chamindra G., Freyermuth, Fernande, Winder, Thomas L., Lawlor, Michael W., Lagier-Tourenne, Clotilde, Patel, Shailendra B.Volume:
5
Language:
english
Journal:
Molecular Genetics & Genomic Medicine
DOI:
10.1002/mgg3.325
Date:
November, 2017
File:
PDF, 2.20 MB
english, 2017