相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。DEPDC5 Mutations in Genetic Focal Epilepsies of Childhood
Dennis Lal et al.
ANNALS OF NEUROLOGY (2014)
XLID-Causing Mutations and Associated Genes Challenged in Light of Data From Large-Scale Human Exome Sequencing
Amelie Piton et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2013)
Tubacin prevents neuronal migration defects and epileptic activity caused by rat Srpx2 silencing in utero
Manal Salmi et al.
BRAIN (2013)
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes
Johannes R. Lemke et al.
NATURE GENETICS (2013)
GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction
Gaetan Lesca et al.
NATURE GENETICS (2013)
GRIN2A mutations cause epilepsy-aphasia spectrum disorders
Gemma L. Carvill et al.
NATURE GENETICS (2013)
Rare Complete Knockouts in Humans: Population Distribution and Significant Role in Autism Spectrum Disorders
Elaine T. Lim et al.
NEURON (2013)
RBFOX1 and RBFOX3 Mutations in Rolandic Epilepsy
Dennis Lal et al.
PLOS ONE (2013)
The Human Language-Associated Gene SRPX2 Regulates Synapse Formation and Vocalization in Mice
G. M. Sia et al.
SCIENCE (2013)
Clinical genetic studies in benign childhood epilepsy with centrotemporal spikes
Danya F. Vears et al.
EPILEPSIA (2012)
PCSK6 is associated with handedness in individuals with dyslexia
Thomas S. Scerri et al.
HUMAN MOLECULAR GENETICS (2011)
Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex
Patrice Roll et al.
HUMAN MOLECULAR GENETICS (2010)
Elongator Controls the Migration and Differentiation of Cortical Neurons through Acetylation of α-Tubulin
Catherine Creppe et al.
CELL (2009)
Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4)
Lisa J. Strug et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2009)
SRPX2 mutations in disorders of language cortex and cognition
P Roll et al.
HUMAN MOLECULAR GENETICS (2006)
A forkhead-domain gene is mutated in a severe speech and language disorder
CSL Lai et al.
NATURE (2001)
分享论文
