Myotonic dystrophy

Author:

Turner Chris,Hilton-Jones David

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical),Neurology

Reference78 articles.

1. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3-prime end of a transcript encoding a protein kinase family member.;Brook;Cell,1992

2. Frequency and stability of the myotonic dystrophy type 1 premutation.;Martorell;Neurology,2001

3. 1, Serrenti M, Meloni C, et al. Triplet-primed PCR is more sensitive than southern blotting-long PCR for the diagnosis of myotonic dystrophy type1.;Addis;Genet Test Mol Biomarkers,2012

4. Myotonic dystrophy: the correlation of (CTG) repeat length in leucocytes with age at onset is significant only for patients with small expansions.;Hamshere;J Med Genet,1999

5. Myotonic dystrophy: size- and sex-dependent dynamics of CTG meiotic instability, and somatic mosaicism.;Lavedan;Am J Hum Genet,1993

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