Expanding the Phenotype and Genetic Defects Associated with the <i>GOSR2</i> Gene.

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第一作者： Roman,Praschberger

第一单位： Department of Molecular Neuroscience UCL Institute of Neurology and The National Hospital for Neurology and Neurosurgery (NHNN) London United Kingdom.

作者： Roman,Praschberger ^[1] ; Bettina,Balint ^[2] ; Niccolo E,Mencacci ^[3] ; Joshua,Hersheson ^[4] ; Ignacio,Rubio-Agusti ^[1] ; Dimitri M,Kullmann ^[1] ; Conceição,Bettencourt ^[5] ; Kailash,Bhatia ^[2] ; Henry,Houlden ^[1]

作者单位： Department of Molecular Neuroscience UCL Institute of Neurology and The National Hospital for Neurology and Neurosurgery (NHNN) London United Kingdom. ^[1] Department of Clinical and Experimental Epilepsy UCL Institute of Neurology London United Kingdom. ^[2] Sobell Department of Motor Neuroscience and Movement Disorders UCL Institute of Neurology London United Kingdom. ^[3] Department of Neurology University Hospital Heidelberg Heidelberg Germany. ^[4] Unidad de Trastornos del Movimiento Hospital Universitario La Fe Valencia Spain. ^[5]

关键词 GOSR2 ataxia myoclonus progressive myoclonus ataxia progressive myoclonus epilepsy

DOI 10.1002/mdc3.12190

PMID 30363482

发布时间 2022-03-21

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Movement disorders clinical practice

2015年2卷3期

271-273页

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Expanding the Phenotype and Genetic Defects Associated with the <i>GOSR2</i> Gene.

Movement disorders clinical practice

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Movement disorders clinical practice

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Expanding the Phenotype and Genetic Defects Associated with the <i>GOSR2</i> Gene.

Movement disorders clinical practice

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Movement disorders clinical practice

相关期刊

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