The long and winding road to personalized medicine in KCNMA1-linked channelopathies revealed by novel variants associated with the Liang-Wang syndrome

Acta Physiol (Oxf). 2022 Aug;235(4):e13854. doi: 10.1111/apha.13854. Epub 2022 Jun 28.

Authors

Maria Virginia Soldovieri¹, Maurizio Taglialatela²

Affiliations

¹ Department of Medicine and Health Sciences "Vincenzo Tiberio", University of Molise, Campobasso, Italy.
² Department of Neuroscience, University of Naples "Federico II", Naples, Italy.

PMID: 35730691
DOI: 10.1111/apha.13854

No abstract available

Publication types

Editorial

MeSH terms

Channelopathies* / genetics
Humans
Large-Conductance Calcium-Activated Potassium Channel alpha Subunits* / genetics
Precision Medicine

Substances

KCNMA1 protein, human
Large-Conductance Calcium-Activated Potassium Channel alpha Subunits