A glycine transporter SLC6A5 frameshift mutation causes startle disease in Spanish greyhounds
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/s00439-019-01986-x.pdf
Reference22 articles.
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3. Eulenburg V, Becker K, Gomeza J, Schmitt B, Becker CM, Betz H (2006) Mutations within the human GLYT2 (SLC6A5) gene associated with hyperekplexia. Biochem Biophys Res Commun 348(2):400–405
4. Fox JG, Averill DR, Hallett M, Schunk K (1984) Familial reflex myoclonus in Labrador Retrievers. Am J Vet Res 45(11):2367–2370
5. Gill JL, Capper D, Vanbellinghen JF, Chung SK, Higgins RJ, Rees MI, Shelton GD, Harvey RJ (2011) Startle disease in Irish wolfhounds associated with a microdeletion in the glycine transporter GlyT2 gene. Neurobiol Dis 43(1):184–189
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