Connexin Mutations and Hereditary Diseases

Inherited diseases caused by connexin mutations are found in multiple organs and include hereditary deafness, congenital cataract, congenital heart diseases, hereditary skin diseases, and X-linked Charcot–Marie–Tooth disease (CMT1X). A large number of knockout and knock-in animal models have been us...

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Detalles Bibliográficos
Autores principales: Qiu, Yue, Zheng, Jianglin, Chen, Sen, Sun, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9027513/
https://www.ncbi.nlm.nih.gov/pubmed/35457072
http://dx.doi.org/10.3390/ijms23084255

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9027513/
https://www.ncbi.nlm.nih.gov/pubmed/35457072
http://dx.doi.org/10.3390/ijms23084255

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