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Genomic structure of postsynaptic organizational protein, Gephyrin, and mutation analysis in hyperekplexia and startle phenotypes

Russell G Snell, Jan Miller, Mike J Owen, Mark Rees

American Journal of Human Genetics, Volume: 67, Issue: 4, Pages: 385 - 386

Swansea University Author: Mark Rees

Published in: American Journal of Human Genetics
Published: 2000
URI: https://cronfa.swan.ac.uk/Record/cronfa21102
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first_indexed 2015-05-07T02:10:08Z
last_indexed 2018-02-09T04:58:18Z
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spelling 2015-05-06T11:35:06.0380984 v2 21102 2015-05-06 Genomic structure of postsynaptic organizational protein, Gephyrin, and mutation analysis in hyperekplexia and startle phenotypes 10f39a4e9c2ee00d453cd84c10667ac8 Mark Rees Mark Rees true false 2015-05-06 BMS Journal Article American Journal of Human Genetics 67 4 385 386 31 12 2000 2000-12-31 COLLEGE NANME Biomedical Sciences COLLEGE CODE BMS Swansea University 2015-05-06T11:35:06.0380984 2015-05-06T11:33:54.7130696 Faculty of Medicine, Health and Life Sciences Swansea University Medical School - Medicine Russell G Snell 1 Jan Miller 2 Mike J Owen 3 Mark Rees 4
title Genomic structure of postsynaptic organizational protein, Gephyrin, and mutation analysis in hyperekplexia and startle phenotypes
spellingShingle Genomic structure of postsynaptic organizational protein, Gephyrin, and mutation analysis in hyperekplexia and startle phenotypes
Mark Rees
title_short Genomic structure of postsynaptic organizational protein, Gephyrin, and mutation analysis in hyperekplexia and startle phenotypes
title_full Genomic structure of postsynaptic organizational protein, Gephyrin, and mutation analysis in hyperekplexia and startle phenotypes
title_fullStr Genomic structure of postsynaptic organizational protein, Gephyrin, and mutation analysis in hyperekplexia and startle phenotypes
title_full_unstemmed Genomic structure of postsynaptic organizational protein, Gephyrin, and mutation analysis in hyperekplexia and startle phenotypes
title_sort Genomic structure of postsynaptic organizational protein, Gephyrin, and mutation analysis in hyperekplexia and startle phenotypes
author_id_str_mv 10f39a4e9c2ee00d453cd84c10667ac8
author_id_fullname_str_mv 10f39a4e9c2ee00d453cd84c10667ac8_***_Mark Rees
author Mark Rees
author2 Russell G Snell
Jan Miller
Mike J Owen
Mark Rees
format Journal article
container_title American Journal of Human Genetics
container_volume 67
container_issue 4
container_start_page 385
publishDate 2000
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
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active_str 0
published_date 2000-12-31T03:24:59Z
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