A transient hyperekplexia phenotype associated with compound heterozygote mutations in the human [Beta]-subunit of the Inhibitory Glycine Receptor (GLRB)

Authors :: Rees, M.I.
Lewis, T.M.
Mortier, G.
Snell, R.G.
Schofield, P.R.
Owen, M.J.
Source :: American Journal of Human Genetics. Oct, 2000, Vol. 67 Issue 4, 391
Publication Year :: 2000

Subjects :: Genetic research -- Analysis
Human genetics -- Research
Genetic disorders -- Research
Biological sciences

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