Referenced in: none

Automatically associated channels: Kir2.3 , Kir6.2 , Slo1

Title: Dominant and recessive central core disease associated with RYR1 mutations and fetal akinesia.

Authors: Norma Beatriz Romero, Nicole Monnier, Louis Viollet, Anne Cortey, Martine Chevallay, Jean Paul Leroy, Joël Lunardi, Michel Fardeau

Journal, date & volume: Brain, 2003 Nov , 126, 2341-9

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/12937085

Abstract