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 gene were...

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Detalhes bibliográficos

Publicado no:	J Med Genet
Principais autores:	Shaw, D J, Chaudhary, S, Rundle, S A, Crow, S, Brook, J D, Harper, P S, Harley, H G
Formato:	Artigo
Idioma:	Inglês
Publicado em:	BMJ Publishing Group 1993
Assuntos:	Research Article
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1016296/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8097255/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.30.3.189
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