An additional family with Startle disease and a G1192A mutation at the α1 subunit of the inhibitory glycine receptor gene
- 1 July 1994
- journal article
- case report
- Published by Oxford University Press (OUP) in Human Molecular Genetics
- Vol. 3 (7) , 1201
- https://doi.org/10.1093/hmg/3.7.1201
Abstract
Daniel F.Schorderet, Graziano Pescia, Andrea Bernasconi, Franco Regli; An additional family with Startle disease and a G1192A mutation at the α1 subunit of theKeywords
This publication has 0 references indexed in Scilit: