HIGHLIGHTS
- who: BIN et al. from the Centronuclear myopathy (CNM) is a genetically heterogeneous congenital myopathy patients (mean age = , ± , years, range, % males) from the Netherlands have published the Article: Clinical, genetic, and histological features of centronuclear myopathy in the Netherlands, in the Journal: Neurology
- what: The authors will discuss the most important findings for each genotype in the following section. mated prevalence of CNM in Europe, predicted by the model of Vandersmissen et_al18: MTM1 variants were considered most prevalent (56%), followed by DNM2 and RYR1 variants (both 12%), and, 18 least commonly, autosomal dominant BIN1 variants . . .
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