Rare variant burden analysis within enhancers identifies CAV1 as an ALS risk gene

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Detalles Bibliográficos
Autores principales: Cooper-Knock, Johnathan, Zhang, Sai, Kenna, Kevin P., Moll, Tobias, Franklin, John P., Allen, Samantha, Nezhad, Helia Ghahremani, Iacoangeli, Alfredo, Yacovzada, Nancy Y., Eitan, Chen, Hornstein, Eran, Elhaik, Eran, Celadova, Petra, Bose, Daniel, Farhan, Sali, Fishilevich, Simon, Lancet, Doron, Morrison, Karen E., Shaw, Christopher E., Al-Chalabi, Ammar, Veldink, Jan H., Kirby, Janine, Snyder, Michael P., Shaw, Pamela J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2021
Materias:
Correction
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7856549/
https://www.ncbi.nlm.nih.gov/pubmed/33535055
http://dx.doi.org/10.1016/j.celrep.2021.108730

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7856549/
https://www.ncbi.nlm.nih.gov/pubmed/33535055
http://dx.doi.org/10.1016/j.celrep.2021.108730

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