Congenital myopathy-causing tropomyosin mutations induce thin filament dysfunction via distinct physiological mechanisms
Ochala, J., Gokhin, D. S., Penisson-Besnier, I., Quijano-Roy, S., Monnier, N., Lunardi, J., Romero, N. B., Fowler, V. M.Volume:
21
Language:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/dds289
Date:
October, 2012
File:
PDF, 451 KB
english, 2012