DMPK hypermethylation in sperm cells of myotonic dystrophy type 1 patients

Myotonic dystrophy type 1 (DM1) is an autosomal dominant muscular dystrophy that results from a CTG expansion (50–4000 copies) in the 3′ UTR of the DMPK gene. The disease is classified into four or five somewhat overlapping forms, which incompletely correlate with expansion size in somatic cells of...

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Detalles Bibliográficos
Autores principales: Yanovsky-Dagan, Shira, Cohen, Eliora, Megalli, Pauline, Altarescu, Gheona, Schonberger, Oshrat, Eldar-Geva, Talia, Epsztejn-Litman, Silvina, Eiges, Rachel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Brief Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9349176/
https://www.ncbi.nlm.nih.gov/pubmed/34776509
http://dx.doi.org/10.1038/s41431-021-00999-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9349176/
https://www.ncbi.nlm.nih.gov/pubmed/34776509
http://dx.doi.org/10.1038/s41431-021-00999-3

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