Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing Analysis
Lu, Yan, Da, Yu-Wei, Zhang, Yong-Biao, Li, Xin-Gang, Wang, Min, Di, Li, Pang, Mi, Lei, LinVolume:
12
Language:
english
Journal:
Frontiers in Neuroscience
DOI:
10.3389/fnins.2018.00329
Date:
May, 2018
File:
PDF, 1.25 MB
english, 2018