miRNome profiling in Duchenne muscular dystrophy; identification of asymptomatic and manifesting female carriers

Duchenne muscular dystrophy (DMD) is a fatal neuromuscular disorder that occurs due to inactivating mutations in DMD gene, leading to muscular dystrophy. Prediction of pathological complications of DMD and the identification of female carriers are important research points that aim to reduce disease...

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Detalles Bibliográficos
Autores principales: Mousa, Nahla O., Sayed, Ahmed A., Fahmy, Nagia, Elzayat, Mariam G., Bakry, Usama, Abdellatif, Ahmed, Zahra, Waheed K., Osman, Ahmed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2021
Materias:
Bioinformatics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450315/
https://www.ncbi.nlm.nih.gov/pubmed/34472584
http://dx.doi.org/10.1042/BSR20211325

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450315/
https://www.ncbi.nlm.nih.gov/pubmed/34472584
http://dx.doi.org/10.1042/BSR20211325

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