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J-GLOBAL ID:201702221186803885
整理番号:17A1479897
GRM1の優性変異は脊髄小脳失調症44型を引き起こす【Powered by NICT】
Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44
著者 (16件):
Watson Lauren M.
(Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford OX1 3PT, UK)
,
Bamber Elizabeth
(Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford OX1 3PT, UK)
,
Schnekenberg Ricardo Parolin
(Nuffield Department of Clinical Neurosciences, University of Oxford, 6th Floor West Wing, John Radcliffe Hospital, Oxford OX3 9DU, UK)
,
Williams Jonathan
(Oxford Medical Genetics Laboratories, Churchill Hospital, Oxford OX3 7LE, UK)
,
Bettencourt Conceicao
(Department of Molecular Neuroscience, Institute of Neurology, University College London, London WC1N 3BG, UK)
,
Bettencourt Conceicao
(Department of Clinical and Experimental Epilepsy, Institute of Neurology, University College London, London WC1N 3BG, UK)
,
Lickiss Jennifer
(West Midlands Regional Genetics Laboratory, Birmingham Women’s and Children’s NHS Foundation Trust, Birmingham B15 2TG, UK)
,
Fawcett Katherine
(MRC Computational Genomics Analysis and Training Programme, MRC Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Oxford OX3 9DS, UK)
,
Clokie Samuel
(West Midlands Regional Genetics Laboratory, Birmingham Women’s and Children’s NHS Foundation Trust, Birmingham B15 2TG, UK)
,
Wallis Yvonne
(West Midlands Regional Genetics Laboratory, Birmingham Women’s and Children’s NHS Foundation Trust, Birmingham B15 2TG, UK)
,
Clouston Penny
(Oxford Medical Genetics Laboratories, Churchill Hospital, Oxford OX3 7LE, UK)
,
Sims David
(MRC Computational Genomics Analysis and Training Programme, MRC Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Oxford OX3 9DS, UK)
,
Houlden Henry
(Department of Molecular Neuroscience, Institute of Neurology, University College London, London WC1N 3BG, UK)
,
Becker Esther B.E.
(Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford OX1 3PT, UK)
,
Nemeth Andrea H.
(Nuffield Department of Clinical Neurosciences, University of Oxford, 6th Floor West Wing, John Radcliffe Hospital, Oxford OX3 9DU, UK)
,
Nemeth Andrea H.
(Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Trust, Oxford OX3 7HE, UK)
資料名:
American Journal of Human Genetics
(American Journal of Human Genetics)
巻:
101
号:
3
ページ:
451-458
発行年:
2017年
JST資料番号:
B0360B
ISSN:
0002-9297
資料種別:
逐次刊行物 (A)
記事区分:
原著論文
発行国:
オランダ (NLD)
言語:
英語 (EN)