Article
Mutation spectrum of hereditary myopathies in Turkish patients and novel variants.
Annals of human genetics - 1 Sept 2021
Saat Hanife, Sahin Ibrahim
Abstract excerpt
Hereditary myopathies are a heterogeneous disorder known to be associated with more than 100 genes. Although hereditary myopathy subgroups can be partially described with traditional methods such as muscle biopsy, next-generation sequencing (NGS) is essential to reveal the disease's underlying genetic etiology and molecular mechanisms. In this study, we performed clinical exome sequencing or whole-exome...
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