Functional characterisation of p.Trp284Ser STAC3 mutation...

Neuromuscular Disorders 2017 / 10 Vol. 27

Functional characterisation of p.Trp284Ser STAC3 mutation causing impaired excitation-contraction coupling in congenital myopathy patients

Zaharieva, I., Sarkozy, A., Manzur, A., Munot, P., Jungbluth, H., Feng, L., Phadke, R., Sewry, C., Treves, S., Muntoni, F.
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Volume:
27
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2017.06.480
Date:
October, 2017
File:
PDF, 244 KB
english, 2017
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