A study of DNA methylation in myotonic dystrophy.

We have examined the hypothesis that the severe congenital form of myotonic dystrophy is caused by genomic imprinting at the level of differential DNA methylation of maternal and paternal alleles. Probes encompassing the 5', central, and 3' regions of the myotonic dystrophy protein kinase...

Full description

Saved in:
Bibliographic Details
Main Authors: Shaw, D J, Chaudhary, S, Rundle, S A, Crow, S, Brook, J D, Harper, P S, Harley, H G
Format: Artigo
Language:Inglês
Published: 1993
Subjects:
Research Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC1016296/
https://ncbi.nlm.nih.gov/pubmed/8097255
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items