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Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the α
<sub/>1</sub>
subunit of the inhibitory glycine receptor

Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the α ₁ subunit of the inhibitory glycine receptor

Rees, Mark I.; Andrew, Martin; Jawad, Sudad; Owen, Michael J.

期刊名称Human Molecular Genetics
作者Rees, Mark I.; Andrew, Martin; Jawad, Sudad; Owen, Michael J.
卷第3卷
期第12期
印刷ISSN0964-6906
电子ISSN1460-2083
文件大小643.36KB
发表时间1994
DOI10.1093/hmg/3.12.2175
页码2175-2179

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