Journal article
Next-Generation Sequencing to Diagnose Muscular Dystrophy, Rhabdomyolysis, and HyperCKemia
Abstract
BACKGROUND: Neuromuscular disorders are a phenotypically and genotypically diverse group of diseases that can be difficult to diagnose accurately because of overlapping clinical features and nonspecific muscle pathology. Next-generation sequencing (NGS) is a high-throughput technology that can be used as a more time- and cost-effective tool for identifying molecular diagnoses for complex genetic conditions, such as neuromuscular disorders.
Authors
Wu L; Brady L; Shoffner J; Tarnopolsky MA
Journal
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, Vol. 45, No. 3, pp. 262–268
Publisher
Cambridge University Press (CUP)
Publication Date
5 2018
DOI
10.1017/cjn.2017.286
ISSN
0317-1671