Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the α1 subunit of the inhibitory glycine receptor-Reference-Cited by-同舟云学术

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Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the α1 subunit of the inhibitory glycine receptor

Published:1994 Issue:12 Volume:3 Page:2175-2179
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum Mol Genet

Author:

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

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/3/12/2175/1831364/3-12-2175.pdf

Cited by 131 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

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3. A novel nonsense autosomal dominant mutation in the GLRA1 gene causing hyperekplexia;Journal of Neural Transmission;2018-09-04

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