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Analysis of GLRA1 in hereditary and sporadic hyperekplexia: A novel mutation in a family cosegregating for hyperekplexia and spastic paraparesis

Elmslie, FV; Hutchings, SM; Spencer, V; Curtis, A; Covanis, T; Gardiner, RM; Rees, M (1996) Analysis of GLRA1 in hereditary and sporadic hyperekplexia: A novel mutation in a family cosegregating for hyperekplexia and spastic paraparesis. JOURNAL OF MEDICAL GENETICS, 33 (5). 435 - 436 (2). ISSN 0022-2593 https://doi.org/10.1136/jmg.33.5.435
SGUL Authors: Elmslie, Frances

Full text not available from this repository.
Item Type: Article
Additional Information: PubMed ID: 8733061
Keywords: Base Sequence, DNA Primers, Female, Humans, Male, Molecular Sequence Data, Movement Disorders, Muscle Hypertonia, Mutation, Pedigree, Receptors, Glycine, Startle Reaction, Science & Technology, Life Sciences & Biomedicine, Genetics & Heredity, hyperekplexia, glycine receptor, GLRA1, STARTLE DISEASE, DOMINANT, hyperekplexia, glycine receptor, GLRA1
Journal or Publication Title: JOURNAL OF MEDICAL GENETICS
ISSN: 0022-2593
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Dates:
DateEvent
1 May 1996Published
Web of Science ID: WOS:A1996UJ32900021
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URI: http://sgultest.da.ulcc.ac.uk/id/eprint/19
Publisher's version: https://doi.org/10.1136/jmg.33.5.435

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