Functional Investigation of a GRIN2A Variant Associated with Rolandic Epilepsy.

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Functional Investigation of a GRIN2A Variant Associated with Rolandic Epilepsy.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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Functional Investigation of a GRIN2A Variant Associated with Rolandic Epilepsy.

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Functional Investigation of a GRIN2A Variant Associated with Rolandic Epilepsy.

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Functional Investigation of a GRIN2A Variant Associated with Rolandic Epilepsy.

@en

Functional Investigation of a GRIN2A Variant Associated with Rolandic Epilepsy.

@nl

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Functional Investigation of a GRIN2A Variant Associated with Rolandic Epilepsy.

@en

Functional Investigation of a GRIN2A Variant Associated with Rolandic Epilepsy.

@nl

P1476

Functional Investigation of a GRIN2A Variant Associated with Rolandic Epilepsy.

@en

P2093

Cui-Ying Fan

http://www.w3.org/2001/XMLSchema#string

Jian-Hong Luo

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Jin-Xing Lai

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Jun-Yu Xu

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Tao Su

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Wei Yang

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Wei-Ping Liao

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Xiao-Rong Liu

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Xing-Xing Xu

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Yi-Wu Shi

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P2860

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GRIN1 mutations cause encephalopathy with infantile-onset epilepsy, and hyperkinetic and stereotyped movement disorders.

Voltage-dependent block by Mg2+ of NMDA responses in spinal cord neurones.

Whole-exome sequencing in an individual with severe global developmental delay and intractable epilepsy identifies a novel, de novo GRIN2A mutation.

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P2888

s12264-017-0182-6

P31

scholarly article

P356

10.1007/S12264-017-0182-6

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P577

2017-09-21T00:00:00Z

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P698

28936771

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P932

5856713

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