المؤلفون: Voermans, Nicol C., Oldfors, Anders, 1951, Jungbluth, Heinz

المصدر: Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease, Seventh Edition: Volume 2. :575-587

مصطلحات موضوعية: Clinical Medicine, Klinisk medicin, central core disease (CCD), congenital fiber-type disproportion (CFTD), Congenital myopathy (CM), multiminicore disease (MmD), myotubular/centronuclear myopathy (MTM/CNM), nemaline myopathy (NM), skeletal muscle ryanodine receptor (RYR1) gene, titin (TTN) gene

URL الوصول: https://gup.ub.gu.se/publication/346186