Muscle weakness in myotonic dystrophy associated with misregulated splicing and altered gating of CaV1.1 calcium channel-Reference-Cited by-同舟云学术

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Muscle weakness in myotonic dystrophy associated with misregulated splicing and altered gating of CaV1.1 calcium channel

Published:2011-12-02 Issue:6 Volume:21 Page:1312-1324
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Tang Zhen Zhi,Yarotskyy Viktor,Wei Lan,Sobczak Krzysztof,Nakamori Masayuki,Eichinger Katy,Moxley Richard T.,Dirksen Robert T.,Thornton Charles A.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/21/6/1312/17258410/ddr568.pdf

Reference75 articles.

1. Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population;Norwood;Brain,2009

2. 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

3. Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9;Liquori;Science,2001

4. Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy;Miller;EMBO J.,2000

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