AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-Acetylaspartate (Q34422339)

2 August 2017

title

AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-Acetylaspartate (English)

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epileptic encephalopathy with global cerebral demyelination

2 August 2017

main subject

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corrigendum / erratum

Erratum to: AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-Acetylaspartate.

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author

Marni Falk

1

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4 June 2020

Francescomassimo Lasorsa

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Hakon Hakonarson

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author name string

Dong Li

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Xiaowu Gai

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Elizabeth McCormick

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Emily Place

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Frederick G Otieno

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Cuiping Hou

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Cecilia E Kim

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Nada Abdel-Magid

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Lyam Vazquez

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Frank D Mentch

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Rosetta Chiavacci

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Jinlong Liang

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Xuanzhu Liu

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Hui Jiang

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Giulia Giannuzzi

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Eric D Marsh

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Guo Yiran

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Lifeng Tian

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Ferdinando Palmieri

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language of work or name

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11 February 2014

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Journal of Inherited Metabolic Disorders Reports

2 August 2017

published in

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volume

14

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page(s)

77-85

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SLC25A22 is a novel gene for migrating partial seizures in infancy.

4 June 2020

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Identifiers

DOI

10.1007/8904_2013_287

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