Journal article 1408 views
A Novel GABRG2 mutation, p.R136*, in a family with GEFS+ and extended phenotypes
Ann J Johnston,
Jing-Qiong Kang,
Wangzhen Shen,
William O Pickrell,
Thomas D Cushion,
Jeffrey Davies 
,
Kristin Baer,
Jonathan Mullins ,
Carrie L Hammond,
Seo-Kyung Chung ,
Rhys H Thomas,
Cathy White,
Phil E.M Smith,
Robert L Macdonald,
Mark Rees,
Owen Pickrell
,
Kristin Baer,
Jonathan Mullins ,
Carrie L Hammond,
Seo-Kyung Chung ,
Rhys H Thomas,
Cathy White,
Phil E.M Smith,
Robert L Macdonald,
Mark Rees,
Owen Pickrell
Neurobiology of Disease
Swansea University Authors:
Jeffrey Davies , Jonathan Mullins , Seo-Kyung Chung , Mark Rees, Owen Pickrell
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DOI (Published version): 10.1016/j.nbd.2013.12.013
Abstract
A Novel GABRG2 mutation, p.R136*, in a family with GEFS+ and extended phenotypes
| Published in: | Neurobiology of Disease |
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| Published: |
2014
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| URI: | https://cronfa.swan.ac.uk/Record/cronfa17001 |
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| College: |
Faculty of Medicine, Health and Life Sciences |
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