Proximal myotonic myopathy syndrome in the absence of trinucleotide repeat expansions
- 1 July 1995
- journal article
- case report
- Published by Wiley in Muscle & Nerve
- Vol. 18 (7) , 782-783
- https://doi.org/10.1002/mus.880180716
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
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- Proximal weakness as the primary manifestation of myotonic dystrophy in older adultsMuscle & Nerve, 1994
- Myotonic dystrophy with no trinucleotide repeat expansionAnnals of Neurology, 1994
- An Unstable Triplet Repeat in a Gene Related to Myotonic Muscular DystrophyScience, 1992
- Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family memberPublished by Elsevier ,1992
- Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19Human Genetics, 1986