Myotonic Dystrophy Type 1 or Steinert’s Disease-Reference-Cited by-同舟云学术

Myotonic Dystrophy Type 1 or Steinert’s Disease

Published:2012 Issue: Volume: Page:239-257
ISSN:0065-2598
Container-title:Advances in Experimental Medicine and Biology
language:
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Author:

Romeo Vincenzo

Publisher

Springer US

Link

http://link.springer.com/content/pdf/10.1007/978-1-4614-0653-2_18.pdf

Reference26 articles.

1. Harper PS. Myotonic dystrophy. Ed. W. B. Saunders, third edition.

2. Brook JD, McCurrach ME, Harley HG et al. 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; 68:799–808.

3. Liquori CL, Ricker K, Moseley ML et al. Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9. Science 2001; 293:864–867.

4. Lavedan C, Hofmann-Radvanyi H, Shelbourne P et al. Myotonic dystrophy: size-and sex-dependent dynamics of CTG meiotic instability and somatic mosaicism. Am J Hum Genet 1993; 52:875–883.

5. Thornton CA, Griggs RC, Moxley RT 3rd. Myotonic dystrophy with no trinucleotide repeat expansion. Ann Neurol 1994; 35:269–272.

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