4.7 Article

Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathy

期刊

ANNALS OF NEUROLOGY
卷 71, 期 3, 页码 407-416

出版社

WILEY-BLACKWELL
DOI: 10.1002/ana.22683

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资金

  1. BJC Institute for Clinical and Translational Sciences
  2. Children's Discovery Institute, National Institutes of Health (NIH) [NINDS NS055980, NS069669, NINDS NS075094, NIA AG031867]
  3. Neuroscience Blueprint Core [NS057105]
  4. Hope Center for Neurological Disorders
  5. Muscular Dystrophy Association [35438, 114845]
  6. NCI Cancer Center [P30 CA91842]
  7. ICTS/CTSA from the National Center for Research Resources (NCRR) [UL1RR024992]

向作者/读者索取更多资源

Objective: To identify the causative gene in an autosomal dominant limb-girdle muscular dystrophy (LGMD) with skeletal muscle vacuoles.

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