Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/145530/1/ana25272_am.pdfhttps://deepblue.lib.umich.edu/bitstream/2027.42/145530/2/ana25272.pd
Mutations in the disheveled, Egl-10 and domain-containing protein 5 (DEPDC5) recently have been iden...
International audienceDEP-domain containing 5 (DEPDC5), encoding a repressor of the mechanistic targ...
International audienceGenetic malformations of cortical development (MCDs), such as mild MCDs (mMCD)...
Epileptogenic mechanisms in focal cortical dysplasia (FCD) remain elusive, as no animal models faith...
Objective: The DEPDC5 (DEP domain-containing protein 5) gene, encoding a repressor of the mTORC1 sig...
Whole-exome sequencing of two brothers with drug-resistant, early-onset, focal epilepsy secondary to...
© 2021 Wei Shern LeeFocal Cortical Dysplasia (FCD) is one of the most common brain malformations and...
AbstractDEP-domain containing 5 (DEPDC5), encoding a repressor of the mechanistic target of rapamyci...
Published online: 03 October 2017DEPDC5 mutations have recently been shown to cause epilepsy in huma...
Type II focal cortical dysplasia (FCD) is a neuropathological entity characterised by cortical dysla...
Epilepsy is a complex disease characterised by seizures due to abnormal neuronal activity. Both here...
Focal cortical dysplasia type 2 (FCD2) is a neurodevelopmental disorder due to mutations in genes of...
Mutations in the GAP activity toward RAGs 1 (GATOR1) complex genes (DEPDC5, NPRL2 and NPRL3) have be...
Introduction: Focal cortical dysplasias (FCDs) are a group of malformations of cortical development ...
Combining human genomics and molecular biology, recent studies have made pivotal progress toward und...
Mutations in the disheveled, Egl-10 and domain-containing protein 5 (DEPDC5) recently have been iden...
International audienceDEP-domain containing 5 (DEPDC5), encoding a repressor of the mechanistic targ...
International audienceGenetic malformations of cortical development (MCDs), such as mild MCDs (mMCD)...
Epileptogenic mechanisms in focal cortical dysplasia (FCD) remain elusive, as no animal models faith...
Objective: The DEPDC5 (DEP domain-containing protein 5) gene, encoding a repressor of the mTORC1 sig...
Whole-exome sequencing of two brothers with drug-resistant, early-onset, focal epilepsy secondary to...
© 2021 Wei Shern LeeFocal Cortical Dysplasia (FCD) is one of the most common brain malformations and...
AbstractDEP-domain containing 5 (DEPDC5), encoding a repressor of the mechanistic target of rapamyci...
Published online: 03 October 2017DEPDC5 mutations have recently been shown to cause epilepsy in huma...
Type II focal cortical dysplasia (FCD) is a neuropathological entity characterised by cortical dysla...
Epilepsy is a complex disease characterised by seizures due to abnormal neuronal activity. Both here...
Focal cortical dysplasia type 2 (FCD2) is a neurodevelopmental disorder due to mutations in genes of...
Mutations in the GAP activity toward RAGs 1 (GATOR1) complex genes (DEPDC5, NPRL2 and NPRL3) have be...
Introduction: Focal cortical dysplasias (FCDs) are a group of malformations of cortical development ...
Combining human genomics and molecular biology, recent studies have made pivotal progress toward und...
Mutations in the disheveled, Egl-10 and domain-containing protein 5 (DEPDC5) recently have been iden...
International audienceDEP-domain containing 5 (DEPDC5), encoding a repressor of the mechanistic targ...
International audienceGenetic malformations of cortical development (MCDs), such as mild MCDs (mMCD)...
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