Novel STMN2 Variant Linked to Amyotrophic Lateral Sclerosis Risk and Clinical Phenotype

OBJECTIVE: There is a critical need to establish genetic markers that explain the complex phenotypes and pathogenicity of ALS. This study identified a polymorphism in the Stathmin-2 gene and investigated its association with sporadic ALS (sALS) disease risk, age-of onset and survival duration. METHO...

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Detalles Bibliográficos
Autores principales: Theunissen, Frances, Anderton, Ryan S., Mastaglia, Frank L., Flynn, Loren L., Winter, Samantha J., James, Ian, Bedlack, Richard, Hodgetts, Stuart, Fletcher, Sue, Wilton, Steve D., Laing, Nigel G., MacShane, Mandi, Needham, Merrilee, Saunders, Ann, Mackay-Sim, Alan, Melamed, Ze’ev, Ravits, John, Cleveland, Don W., Akkari, P. Anthony
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8033025/
https://www.ncbi.nlm.nih.gov/pubmed/33841129
http://dx.doi.org/10.3389/fnagi.2021.658226

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8033025/
https://www.ncbi.nlm.nih.gov/pubmed/33841129
http://dx.doi.org/10.3389/fnagi.2021.658226

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