A missense mutation in the gene encoding the α1 subunit of the inhibitory glycine receptor in the spasmodic mouse-Reference-Cited by-同舟云学术

A missense mutation in the gene encoding the α1 subunit of the inhibitory glycine receptor in the spasmodic mouse

Published:1994-06 Issue:2 Volume:7 Page:131-135
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Ryan Stephen G.,Buckwalter Marion S.,Lynch Joseph W.,Handford Cheryl A.,Segura Lillian,Shiang Rita,Wasmuth John J.,Camper Sally A.,Schofield Peter,O'Connell Peter

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0694-131.pdf

Reference30 articles.

1. Ryan, S.G. et al. Startle disease or hyperekplexia: response to clonazepam and assignment of the gene (STHE) to chromosome 5q by linkage analysis. Ann. Neurol. 31, 663–668 (1992).

2. Nigro, M.A. & Lim, H.-C.N. Hyperekplexia and sudden neonatal death. Pediatr. Neurol. 8, 221–225 (1992).

3. Giacoia, G.P. & Ryan, S.G. Am. J. Dis. Child, (in the press).

4. Andermann, F., Keene, D.L., Andermann, E. & Quesney, L.F. Startle disease or hyperekplexia: further delineation of the syndrome. Brain 103, 985–997 (1980).

5. Morley, D.J., Weaver, D.D. & Garg, B.P. Hyperexplexia: an inherited disorder of the startle response. Clin. Genet. 21, 388–396 (1982).

Cited by 160 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

1. Comprehensive behavioral analyses of mice with a glycine receptor alpha 4 deficiency;Molecular Brain;2023-05-22

2. Glycine receptor autoantibody binding to the extracellular domain is independent from receptor glycosylation;Frontiers in Molecular Neuroscience;2023-02-13

3. Photocontrol of Endogenous Glycine Receptors In Vivo;Cell Chemical Biology;2020-11

4. Anxiety and Startle Phenotypes in Glrb Spastic and Glra1 Spasmodic Mouse Mutants;Frontiers in Molecular Neuroscience;2020-08-11

5. Photocontrol of endogenous glycine receptors in vivo;2019-08-22