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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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Detalhes bibliográficos
Publicado no: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.
Formato: Artigo
Idioma:Inglês
Publicado em: 2015
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Acesso em linha: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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