Molecular Factors Involved in Spinal Muscular Atrophy Pathways as Possible Disease-modifying Candidates

Spinal Muscular Atrophy (SMA) is a neuromuscular disorder caused by mutations in the SMN1 gene. Being a monogenic disease, it is characterized by high clinical heterogeneity. Variations in penetrance and severity of symptoms, as well as clinical discrepancies between affected family members can resu...

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Detalles Bibliográficos
Autores principales: Maretina, Marianna A., Zheleznyakova, Galina Y., Lanko, Kristina M., Egorova, Anna A., Baranov, Vladislav S., Kiselev, Anton V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030859/
https://www.ncbi.nlm.nih.gov/pubmed/30065610
http://dx.doi.org/10.2174/1389202919666180101154916

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030859/
https://www.ncbi.nlm.nih.gov/pubmed/30065610
http://dx.doi.org/10.2174/1389202919666180101154916

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