CpG methylation and various parameters interaction in myotonic dystrophy type 1-Reference-Cited by-同舟云学术

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CpG methylation and various parameters interaction in myotonic dystrophy type 1

Published:2020 Issue:1 Volume:9 Page:16-25
ISSN:2473-0831
Container-title:Journal of Analytical & Pharmaceutical Research
language:
Short-container-title:JAPLR

Author:

Kumar Ashok,Agarwal Sarita,Pradhan Sunil

Publisher

MedCrave Group, LLC

Subject

General Medicine

Reference45 articles.

1. Myotonic Dystrophy;Thornton;Neurol Clin,2014

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

3. 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

4. Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy;Buxton;Nature,1992

5. Best practice guidelines and recommendations on the molecular diagnosis of myotonic dystrophy types 1 and 2;Kamsteeg;Eur J Hum Genet,2012

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