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Myotonic dystrophy
LE WE PMID CA
Myotonic dystrophy1897Myotone Dystrophie

ClC1 Ion channel

CUGBP1

delta Sarcoglycan

DMPK

Dystroglycan

FRA12A mental retardation

Fragile X syndrome

FRAXE mental retardation

Friedreich ataxia

Genetics (Trinucleotide repeat)

Laminin211

Limb girdle muscular dystrophy type 2B

MBNL1

Myotonia

Myotonic dystrophy

RNA (RNA foci)

SCN4A

ZNF9

1966  
1
Myotonia dystrophica: review of 17 patients.
[5909394] South Med J 59(4): 404-7 (1966)
2004  
2
Myotonic dystrophy: RNA pathogenesis comes into focus.
[15065017] Am J Hum Genet 74(5): 793-804 (2004)
2008  
3
2009  
4
Chromatin remodeling in the noncoding repeat expansion diseases.
[18957431] J Biol Chem 284(12): 7413-7 (2009)
2005  
5
2011  
6
Cellular toxicity of expanded RNA repeats: focus on RNA foci.
[21729883] Hum Mol Genet 20(19): 3811-21 (2011)
2010  
7
Molecular therapy in myotonic dystrophy: focus on RNA gain-of-function.
[20406734] Hum Mol Genet 19(R1): R90-7 (2010)
2011  
8
Skeletal muscle laminin and MDC1A: pathogenesis and treatment strategies.
[21798088] Skelet Muscle 1(1): 9 (2011)
2011  
9
δ-Sarcoglycan-deficient muscular dystrophy: from discovery to therapeutic approaches.
[21798091] Skelet Muscle 1(1): 13 (2011)
2010  
10
Myotonic dystrophies 1 and 2: complex diseases with complex mechanisms.
[20885816] Curr Genomics 11(2): 77-90 (2010)
PMC   
11
Diastolic Function in Steinert's Disease.
[24744846] Neurol Int 6(1):5140 (2014)

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All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.


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