Sort   by:  
 Page size 
UnknownLinkage of benign familial infantile convulsions to chromosome 16p12-q12 suggests allelism to the infantile convulsions and choreoathetosis syndrome.
Not available
S-EPMC1274492 | biostudies-literature
UnknownMolecular evolution of the human SRPX2 gene that causes brain disorders of the Rolandic and Sylvian speech areas.
Not available
S-EPMC2151080 | biostudies-literature
UnknownHeterogeneous pattern of selective pressure for PRRT2 in human populations, but no association with autism spectrum disorders.
Not available
S-EPMC3940422 | biostudies-literature
UnknownSpontaneous spike-and-wave discharges during sleep in mice: circadian distribution and impact on sleep quality.
Not available
S-EPMC12855067 | biostudies-literature
UnknownMolecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex.
Not available
S-EPMC2989892 | biostudies-literature
UnknownThe Epilepsy of Infancy With Migrating Focal Seizures: Identification of de novo Mutations of the KCNT2 Gene That Exert Inhibitory Effects on the Corresponding Heteromeric KNa1.1/KNa1.2 Potassium Channel.
Not available
S-EPMC6992647 | biostudies-literature
UnknownLong-term management of leukocyte adhesion deficiency type III without hematopoietic stem cell transplantation.
Not available
S-EPMC6058776 | biostudies-literature
UnknownInfantile convulsions with paroxysmal dyskinesia (ICCA syndrome) and copy number variation at human chromosome 16p11.
Not available
S-EPMC2966418 | biostudies-literature
UnknownHomozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse.
Not available
S-EPMC384949 | biostudies-literature
UnknownLoss of function of the retinoid-related nuclear receptor (RORB) gene and epilepsy.
Not available
S-EPMC5117930 | biostudies-literature
Sort   by:  
 Page size