Two definite cases of sudden unexpected death in epilepsy in a family with a DEPDC5 mutation.
about
Identification of DEP domain-containing proteins by a machine learning method and experimental analysis of their expression in human HCC tissues.DEPDC5 mutations in familial and sporadic focal epilepsy.Epilepsy: Transition from pediatric to adult care. Recommendations of the Ontario epilepsy implementation task force.Whole-exome sequencing in neurologic practice: Reducing the diagnostic odyssey.Genetic Basis of Sudden Unexpected Death in Epilepsy.A mouse model of DEPDC5-related epilepsy: Neuronal loss of Depdc5 causes dysplastic and ectopic neurons, increased mTOR signaling, and seizure susceptibility.The past, present and future challenges in epilepsy related and sudden deaths and biobanking.Involvement of GATOR complex genes in familial focal epilepsies and focal cortical dysplasia.Cardiac arrhythmia and neuroexcitability gene variants in resected brain tissue from patients with sudden unexpected death in epilepsy (SUDEP).Delving Deeper into DEPDC5.
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P2860
Two definite cases of sudden unexpected death in epilepsy in a family with a DEPDC5 mutation.
description
2015 nî lūn-bûn
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2015年の論文
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2015年論文
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2015年論文
@zh-hant
2015年論文
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2015年論文
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2015年論文
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2015年论文
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2015年论文
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2015年论文
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name
Two definite cases of sudden u ...... family with a DEPDC5 mutation.
@en
Two definite cases of sudden u ...... family with a DEPDC5 mutation.
@nl
type
label
Two definite cases of sudden u ...... family with a DEPDC5 mutation.
@en
Two definite cases of sudden u ...... family with a DEPDC5 mutation.
@nl
prefLabel
Two definite cases of sudden u ...... family with a DEPDC5 mutation.
@en
Two definite cases of sudden u ...... family with a DEPDC5 mutation.
@nl
P2093
P2860
P1433
P1476
Two definite cases of sudden u ...... family with a DEPDC5 mutation.
@en
P2093
Berge A Minassian
Danielle M Andrade
Patrick Cossette
P2860
P356
10.1212/NXG.0000000000000028
P577
2015-10-15T00:00:00Z