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...

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Bibliografiska uppgifter
Huvudupphovsmän: Shaw, D J, Chaudhary, S, Rundle, S A, Crow, S, Brook, J D, Harper, P S, Harley, H G
Materialtyp: Artigo
Språk:Inglês
Publicerad: 1993
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC1016296/
https://ncbi.nlm.nih.gov/pubmed/8097255
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