Mutations in the GlyT2 gene (SLC6A5) are a second major cause of startle disease

Carta, E. et al. (2012) Mutations in the GlyT2 gene (SLC6A5) are a second major cause of startle disease. Journal of Biological Chemistry, 287(34), pp. 28975-28985. (doi: 10.1074/jbc.M112.372094)

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Item Type:Articles
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Zuberi, Dr Sameer
Authors: Carta, E., Chung, S.-K., James, V.M., Robinson, A., Gill, J.L., Remy, N., Vanbellinghen, J.-F., Drew, C.J.G., Cagdas, S., Cameron, D., Cowan, F.M., Del Toro, M., Graham, G.E., Manzur, A.Y., Masri, A., Rivera, S., Scalais, E., Shiang, R., Sinclair, K., Stuart, C.A., Tijssen, M.A.J., Wise, G., Zuberi, S.M., Harvey, K., Pearce, B.R., Topf, M., Thomas, R.H., Supplisson, S., Rees, M.I., and Harvey, R.J.
College/School:College of Medical Veterinary and Life Sciences > School of Medicine, Dentistry & Nursing
Journal Name:Journal of Biological Chemistry
Journal Abbr.:J Biol Chem.
ISSN:0021-9258
ISSN (Online):1083-351X

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