Gap Junction Channelopathies and Calmodulinopathies. Do Disease-Causing Calmodulin Mutants Affect Direct Cell–Cell Communication?

The cloning of connexins cDNA opened the way to the field of gap junction channelopathies. Thus far, at least 35 genetic diseases, resulting from mutations of 11 different connexin genes, are known to cause numerous structural and functional defects in the central and peripheral nervous system as we...

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Detalles Bibliográficos
Autor principal: Peracchia, Camillo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8431743/
https://www.ncbi.nlm.nih.gov/pubmed/34502077
http://dx.doi.org/10.3390/ijms22179169

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8431743/
https://www.ncbi.nlm.nih.gov/pubmed/34502077
http://dx.doi.org/10.3390/ijms22179169

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