Mutations in the human skeletal muscle chloride channel gene (CLCN1) associated with dominant and recessive myotonia congenita.

v1

Type:Journal Article

0 views

[![NobleID](https://www.nobleid.org/api/badge/FCA2BA73.svg?ark=w1%2F20260515%2FFCA2BA73)](https://nobleid.org/work/w1/20260515/FCA2BA73)

ARK Inflections

Bibliometric Analysis

Impact metrics, research fronts, co-authorship networks →

Authors & Claims

Paper Authors