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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

Published in: Human Molecular Genetics
Published: 1994
URI: https://cronfa.swan.ac.uk/Record/cronfa20917
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first_indexed 2015-04-29T02:04:02Z
last_indexed 2018-02-09T04:57:55Z
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spelling 2015-04-28T17:28:31.2263730 v2 20917 2015-04-28 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 10f39a4e9c2ee00d453cd84c10667ac8 Mark Rees Mark Rees true false 2015-04-28 BMS Journal Article Human Molecular Genetics 3 12 2175 2179 31 12 1994 1994-12-31 COLLEGE NANME Biomedical Sciences COLLEGE CODE BMS Swansea University 2015-04-28T17:28:31.2263730 2015-04-28T17:25:25.9248218 Faculty of Medicine, Health and Life Sciences Swansea University Medical School - Medicine Mark Rees 1 Mark Andrew 2 Saeed Jawad 3 Mike J Owen 4
title 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
spellingShingle 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
title_short 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
title_full 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
title_fullStr 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
title_full_unstemmed 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
title_sort 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
author_id_str_mv 10f39a4e9c2ee00d453cd84c10667ac8
author_id_fullname_str_mv 10f39a4e9c2ee00d453cd84c10667ac8_***_Mark Rees
author Mark Rees
author2 Mark Rees
Mark Andrew
Saeed Jawad
Mike J Owen
format Journal article
container_title Human Molecular Genetics
container_volume 3
container_issue 12
container_start_page 2175
publishDate 1994
institution Swansea University
college_str Faculty of Medicine, Health and Life Sciences
hierarchytype
hierarchy_top_id facultyofmedicinehealthandlifesciences
hierarchy_top_title Faculty of Medicine, Health and Life Sciences
hierarchy_parent_id facultyofmedicinehealthandlifesciences
hierarchy_parent_title Faculty of Medicine, Health and Life Sciences
department_str Swansea University Medical School - Medicine{{{_:::_}}}Faculty of Medicine, Health and Life Sciences{{{_:::_}}}Swansea University Medical School - Medicine
document_store_str 0
active_str 0
published_date 1994-12-31T03:24:46Z
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score 11.036706

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