Gain-of-function mutations in KCNK3 cause a developmental disorder with sleep apnea. (2022)

First Author: Sörmann J
Attributed to:  Unlocking the Potential of K2P Potassium Channels with Nanobodies funded by BBSRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41588-022-01185-x

PubMed Identifier: 36195757

Publication URI: http://europepmc.org/abstract/MED/36195757

Type: Journal Article/Review

Volume: 54

Parent Publication: Nature genetics

Issue: 10

ISSN: 1061-4036