Abnormal Development of Neural Stem Cell Niche in the Dentate Gyrus of Menkes Disease

BACKGROUND AND OBJECTIVES: Menkes disease (MNK) is a rare X-linked recessive disease, caused by mutations in the copper transporting ATP7A gene that is required for copper homeostasis. MNK patients experience various clinical symptoms including neurological defects that are closely related to the pr...

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Detalles Bibliográficos
Autores principales: Cho, Sung-kuk, Gwon, Suhyun, Kim, Hyun Ah, Kim, Jiwon, Cho, Sung Yoo, Kim, Dong-Eog, Chae, Jong-Hee, Park, Dae Hwi, Hwang, Yu Kyeong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Stem Cell Research 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9396019/
https://www.ncbi.nlm.nih.gov/pubmed/35220279
http://dx.doi.org/10.15283/ijsc21088

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9396019/
https://www.ncbi.nlm.nih.gov/pubmed/35220279
http://dx.doi.org/10.15283/ijsc21088

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