Absence of a differentiation defect in muscle satellite cells from DM2 patients

Myotonic dystrophy type 1 (DM1) and type II (DM2) are dominantly inherited multisystemic disorders. DM1 is triggered by the pathological expansion of a (CTG)n triplet repeat in the DMPK gene, whereas a (CCTG)n tetranucleotide repeat expansion in the ZNF9 gene causes DM2. Both forms of the disease sh...

詳細記述

書誌詳細

主要な著者:	Richard Pelletier, Frederic Hamel, Daniel Beaulieu, Lysanne Patry, Caroline Haineault, Mark Tarnopolsky, Benedikt Schoser, Jack Puymirat
フォーマット:	Artigo
言語:	Inglês
出版事項:	Elsevier 2009-10-01
シリーズ:	Neurobiology of Disease
主題:	Myotonic dystrophy (DM) Proximal myotonic myopathy (PROMM DM2) Proximal myotonic dystrophy DM2 (PDM) Muscle satellite cell CUGBP1 cDM1
オンライン･アクセス:	http://www.sciencedirect.com/science/article/pii/S0969996109001806
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