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
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| 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 |
| Related URLs: |
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| Dates: |
| Date | Event |
|---|
| 1 May 1996 | Published |
|
| Web of Science ID: |
WOS:A1996UJ32900021 |
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| URI: |
https://openaccess.sgul.ac.uk/id/eprint/19 |
| Publisher's version: |
https://doi.org/10.1136/jmg.33.5.435 |
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