Myotonic dystrophies: An update on clinical aspects, genetic, pathology, and molecular pathomechanisms-Reference-Cited by-同舟云学术

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Myotonic dystrophies: An update on clinical aspects, genetic, pathology, and molecular pathomechanisms

Published:2015-04 Issue:4 Volume:1852 Page:594-606
ISSN:0925-4439
Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

Meola Giovanni,Cardani Rosanna

Funder

Centro per lo Studio delle Malattie Neuromuscolari

Fondazione Malattie Miotoniche

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference199 articles.

1. Myotonic dystrophy;Harper,2001

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

3. An unstable triplet repeat in a gene related to myotonic muscular dystrophy;Fu;Science,1992

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

5. Proximal myotonic myopathy: a new dominant disorder with myotonia, muscle weakness, and cataracts;Ricker;Neurology,1994

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