Novel mutation in optineurin causing aggressive ALS+/−frontotemporal dementia

OBJECTIVE: Mutations in optineurin (OPTN) have been identified in familial and sporadic amyotrophic lateral sclerosis (ALS). We screened a cohort of Chinese patients for mutations in optineurin. We also performed an extensive literatures review of all mutations in optineurin identified previously to...

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Detalles Bibliográficos
Autores principales: Feng, Shu‐Man, Che, Chun‐Hui, Feng, Shu‐Yan, Liu, Chang‐Yun, Li, Liu‐Yi, Li, Yuan‐Xiao, Huang, Hua‐Pin, Zou, Zhang‐Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6917321/
https://www.ncbi.nlm.nih.gov/pubmed/31838784
http://dx.doi.org/10.1002/acn3.50928

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6917321/
https://www.ncbi.nlm.nih.gov/pubmed/31838784
http://dx.doi.org/10.1002/acn3.50928

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