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Volumn 56, Issue 10, 2015, Pages e168-e171
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DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy
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Author keywords
Familial focal epilepsy with variable foci; Genetics; Mutation; Temporal lobe seizures
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Indexed keywords
CARBAMAZEPINE;
DEP DOMAIN CONTAINING PROTEIN 5;
LAMOTRIGINE;
MESSENGER RNA;
PHENOBARBITAL;
PROTEIN;
TOPIRAMATE;
UNCLASSIFIED DRUG;
VALPROIC ACID;
DEPDC5 PROTEIN, HUMAN;
REPRESSOR PROTEIN;
ADULT;
ANXIETY DISORDER;
ARTICLE;
AUTOSOMAL DOMINANT DISORDER;
AUTOSOMAL DOMINANT LATERAL TEMPORAL EPILEPSY;
CLINICAL ARTICLE;
DEJA VU;
DISEASE CLASSIFICATION;
DISEASE COURSE;
DISEASE DURATION;
DRUG TREATMENT FAILURE;
ELECTROENCEPHALOGRAPHY;
EXOME;
FAMILIAL DISEASE;
FAMILIAL MESIAL TEMPORAL LOBE EPILEPSY;
FEBRILE CONVULSION;
FEMALE;
FUNCTIONAL NEUROIMAGING;
GENE SEQUENCE;
GENETIC ANALYZER;
GENETIC SCREENING;
GENOME ANALYSIS;
HUMAN;
MALE;
MESIAL TEMPORAL LOBE EPILEPSY;
NONSENSE MUTATION;
NUCLEAR MAGNETIC RESONANCE IMAGING;
ONSET AGE;
PRIORITY JOURNAL;
RNA DEGRADATION;
STOMACH DISEASE;
STOP CODON;
TEMPORAL LOBE EPILEPSY;
TONIC CLONIC SEIZURE;
TREATMENT OUTCOME;
TREATMENT RESPONSE;
FAMILY HEALTH;
GENETICS;
ITALY;
MUTATION;
NUCLEOTIDE SEQUENCE;
ADULT;
DNA MUTATIONAL ANALYSIS;
EPILEPSY, TEMPORAL LOBE;
FAMILY HEALTH;
FEMALE;
HUMANS;
ITALY;
MALE;
MUTATION;
REPRESSOR PROTEINS;
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EID: 84943181104
PISSN: 00139580
EISSN: 15281167
Source Type: Journal
DOI: 10.1111/epi.13094 Document Type: Article |
Times cited : (41)
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References (11)
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