Leukocyte telomere length in patients with myotonic dystrophy type I: a pilot study

Myotonic dystrophy type I (DM1) is an autosomal dominant disease of which clinical manifestations resemble premature aging. We evaluated the contribution of telomere length in pathogenesis in 361 DM1 patients (12 with serial measurements) and 223 unaffected relative controls using qPCR assay. While...

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Detalles Bibliográficos
Autores principales: Wang, Youjin, Best, Ana, Fernández‐Torrón, Roberto, Alsaggaf, Rotana, Garcia‐Puga, Mikel, Dagnall, Casey L., Hicks, Belynda, Thompson, Mone’t, Matheu Fernandez, Ander, Zulaica Ijurco, Miren, Greene, Mark H., Lopez de Munain, Adolfo, Gadalla, Shahinaz M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Brief Communications
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6952307/
https://www.ncbi.nlm.nih.gov/pubmed/31808320
http://dx.doi.org/10.1002/acn3.50954

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6952307/
https://www.ncbi.nlm.nih.gov/pubmed/31808320
http://dx.doi.org/10.1002/acn3.50954

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