Experts has a new look! Let us know what you think of the updates.

Provide feedback
Home
Scholarly Works
Next-Generation Sequencing to Diagnose Muscular...
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