Progressive skeletal muscle weakness in transgenic mice expressing CTG expansions is associated with the activation of the ubiquitin–proteasome pathway-Reference-Cited by-同舟云学术

Progressive skeletal muscle weakness in transgenic mice expressing CTG expansions is associated with the activation of the ubiquitin–proteasome pathway

Published:2010-05 Issue:5 Volume:20 Page:319-325
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Vignaud Alban,Ferry Arnaud,Huguet Aline,Baraibar Martin,Trollet Capucine,Hyzewicz Janek,Butler-Browne Gillian,Puymirat Jack,Gourdon Genevieve,Furling Denis

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference41 articles.

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3. Myotonic dystrophy mutation: an unstable CTG repeat in the 3′ untranslated region of the gene;Mahadevan;Science,1992

4. The correlation of age of onset with CTG trinucleotide repeat amplification in myotonic dystrophy;Hunter;J Med Genet,1992

5. Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy;Tsilfidis;Nat Genet,1992

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