No Cover Image

Journal article 988 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

Published in: Human Molecular Genetics
Published: 1994
URI: https://cronfa.swan.ac.uk/Record/cronfa20917
Tags: Add Tag
No Tags, Be the first to tag this record!
first_indexed 2015-04-29T02:04:02Z
last_indexed 2018-02-09T04:57:55Z
id cronfa20917
recordtype SURis
fullrecord <?xml version="1.0"?><rfc1807><datestamp>2015-04-28T17:28:31.2263730</datestamp><bib-version>v2</bib-version><id>20917</id><entry>2015-04-28</entry><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</title><swanseaauthors><author><sid>10f39a4e9c2ee00d453cd84c10667ac8</sid><ORCID/><firstname>Mark</firstname><surname>Rees</surname><name>Mark Rees</name><active>true</active><ethesisStudent>false</ethesisStudent></author></swanseaauthors><date>2015-04-28</date><deptcode>BMS</deptcode><abstract></abstract><type>Journal Article</type><journal>Human Molecular Genetics</journal><volume>3</volume><journalNumber>12</journalNumber><paginationStart>2175</paginationStart><paginationEnd>2179</paginationEnd><publisher/><keywords/><publishedDay>31</publishedDay><publishedMonth>12</publishedMonth><publishedYear>1994</publishedYear><publishedDate>1994-12-31</publishedDate><doi/><url/><notes></notes><college>COLLEGE NANME</college><department>Biomedical Sciences</department><CollegeCode>COLLEGE CODE</CollegeCode><DepartmentCode>BMS</DepartmentCode><institution>Swansea University</institution><apcterm/><lastEdited>2015-04-28T17:28:31.2263730</lastEdited><Created>2015-04-28T17:25:25.9248218</Created><path><level id="1">Faculty of Medicine, Health and Life Sciences</level><level id="2">Swansea University Medical School - Medicine</level></path><authors><author><firstname>Mark</firstname><surname>Rees</surname><orcid/><order>1</order></author><author><firstname>Mark</firstname><surname>Andrew</surname><order>2</order></author><author><firstname>Saeed</firstname><surname>Jawad</surname><order>3</order></author><author><firstname>Mike J</firstname><surname>Owen</surname><order>4</order></author></authors><documents/><OutputDurs/></rfc1807>
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
_version_ 1763750850045411328
score 11.012678

Similar Items