Targeted sequencing and identification of genetic variants in sporadic inclusion body myositis

Sporadic inclusion body myositis (sIBM) has clinical, pathologic and pathomechanistic overlap with some inherited muscle and neurodegenerative disorders. In this study, DNA from 79 patients with sIBM was collected and the sequencing of 38 genes associated with hereditary inclusion body myopathy (IBM...

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Bibliographic Details
Published in:Neuromuscul Disord
Main Authors: Weihl, Conrad C., Baloh, Robert H., Lee, Youjin, Chou, Tsui-Fen, Pittman, Sara K., Lopate, Glenn, Allred, Peggy, Jockel-Balsarotti, Jennifer, Pestronk, Alan, Harms, Matthew B.
Format: Artigo
Language:Inglês
Published: 2015
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Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4372452/
https://ncbi.nlm.nih.gov/pubmed/25617006
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nmd.2014.12.009
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