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Updated: Jul 20, 2026

09:39
Modeling Myotonic Dystrophy 1 in C2C12 Myoblast Cells
Published on: July 29, 2016
Myotonia congenita in a brother and sister
Tipu Sultan1, Malik Muhammad Nazir Khan, Adeel Humayun
1Department of Neurology, Children Hospital, Institute of Child Health, Lahore. tipusultanmalik@hotmail.com
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP
|September 2, 2006
Abstract:
Myotonia congenita is a rare channelopathy and carries a good prognosis. Two cases of young siblings are presented detected with difficulty in gait and motor activities. Both had typical hypertrophied body musculature. EMG was diagnostic.
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