Clinical and genetic study of a Chinese family affected by both amyotrophic lateral sclerosis and autosomal dominant polycystic kidney disease

Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder characterized by loss of the upper and lower motor neurons from the motor cortex, brainstem, and spinal cord. Most ALS cases are sporadic, with 5–10% having a positive family history. Autosomal dominant polycystic kidney...

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Detalles Bibliográficos
Autores principales: Li, Shirong, Lin, Junyu, Li, Chunyu, Chen, Yongping, Cao, Bei, Yang, Tianmi, Wei, Qianqian, Zhao, Bi, Chen, Xueping, Shang, Huifang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9630937/
https://www.ncbi.nlm.nih.gov/pubmed/36341123
http://dx.doi.org/10.3389/fneur.2022.1004909

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9630937/
https://www.ncbi.nlm.nih.gov/pubmed/36341123
http://dx.doi.org/10.3389/fneur.2022.1004909

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