An additional family with Startle disease and a G1192A mutation at the alpha 1 subunit of the inhibitory glycine receptor gene.

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作者信息

Schorderet D F, Pescia G, Bernasconi A, Regli F

机构信息

Division of Medical Genetics, CHUV, Lausanne, Switzerland.

出版信息

Hum Mol Genet. 1994 Jul;3(7):1201. doi: 10.1093/hmg/3.7.1201.

DOI:10.1093/hmg/3.7.1201

PMID:7981700

Abstract

摘要

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