Journal article 959 views
Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the alpha 1 subunit of the inhibitory glycine receptor
Mark Rees,
Mark Andrew,
Saeed Jawad,
Mike J Owen
Human Molecular Genetics, Volume: 3, Issue: 12, Pages: 2175 - 2179
Swansea University Author: Mark Rees
Abstract
Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the alpha 1 subunit of the inhibitory glycine receptor
| Published in: | Human Molecular Genetics |
|---|---|
| Published: |
1994
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| URI: | https://cronfa.swan.ac.uk/Record/cronfa20917 |
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| College: |
Faculty of Medicine, Health and Life Sciences |
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| Issue: |
12 |
| Start Page: |
2175 |
| End Page: |
2179 |