Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Genetics (clinical),Neurology (clinical)
Reference105 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;Cell,1992
2. Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9;Science,2001
3. Population frequency of myotonic dystrophy: higher than expected frequency of myotonic dystrophy type 2 (DM2) mutation in Finland;Eur J Hum Genet,2011
4. Anatomy of a founder effect: myotonic dystrophy in Northeastern Quebec;Hum Genet,2005
5. Genetic prevalence of myotonic dystrophy type 1;Neurology,2019
Cited by
15 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