Myotonic Dystrophy Type 2: Clinical and Genetic Aspects
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Elsevier
Reference161 articles.
1. Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member;Brook;Cell,1992
2. An unstable triplet repeat in a gene related to myotonic muscular dystrophy;Fu;Science,1992
3. Myotonic dystrophy mutation: An unstable CTG repeat in the 3′ untranslated region of the gene;Mahadevan;Science,1992
4. Proximal myotonic myopathy: A new dominant disorder with myotonia, muscle weakness, and cataracts;Ricker;Neurology,1994
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Population frequency of myotonic dystrophy: higher than expected frequency of myotonic dystrophy type 2 (DM2) mutation in Finland;European Journal of Human Genetics;2011-03-02
2. Altered MEF2 isoforms in myotonic dystrophy and other neuromuscular disorders;Muscle & Nerve;2010-11-22
3. Differences in aberrant expression and splicing of sarcomeric proteins in the myotonic dystrophies DM1 and DM2;Acta Neuropathologica;2010-01-12
4. Genetic instabilities of (CCTG)·(CAGG) and (ATTCT)·(AGAAT) disease-associated repeats reveal multiple pathways for repeat deletion;Molecular Carcinogenesis;2009-04
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