RNA pathogenesis of the myotonic dystrophies-Reference-Cited by-同舟云学术

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RNA pathogenesis of the myotonic dystrophies

Published:2005-01 Issue:1 Volume:15 Page:5-16
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Day John W.,Ranum Laura P.W.

Funder

Muscular Dystrophy Association

National Institutes of Health

Publisher

Elsevier BV

Subject

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

Reference109 articles.

1. Long CTG tracts from the myotonic dystrophy gene induce deletions and rearrangements during recombination at the APRT locus in CHO cells;Meservy;Mol Cell Biol,2003

2. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome;Verkerk;Cell,1991

3. Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy;la Spada;Nature,1991

4. Molecular genetics and pathogenesis of Friedreich ataxia;Pandolfo;Neuromuscul Disord,1998

5. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1;Orr;Nat Genet,1993

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