Neuropathology of 16p13.11 deletion in epilepsy

PLoS ONE

Volumn 7, Issue 4, 2012, Pages

  Liu, Joan Y W ^a   Kasperavičiute, Dalia ^a   Martinian, Lillian ^a   Thom, Maria ^a   Sisodiya, Sanjay M ^a,b  

^a NATIONAL HOSPITAL FOR NEUROLOGY AND NEUROSURGERY   (United Kingdom)

^b EPILEPSY SOCIETY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ANATOMICAL VARIATION; ARTICLE; CASE REPORT; CHROMOSOME 16P; CHROMOSOME 16P13.11; CHROMOSOME DELETION; CONTROLLED STUDY; COPY NUMBER VARIATION; CYTOARCHITECTURE; DISEASE CONTROL; FEMALE; GENE; HETEROZYGOSITY; HIPPOCAMPAL SCLEROSIS; HISTOLOGY; HUMAN; HUMAN CELL; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; MALE; MESIAL TEMPORAL LOBE EPILEPSY; NDE1 GENE; NERVE CELL; NEUROPATHOLOGY; TEMPORAL CORTEX; TEMPORAL LOBE EPILEPSY; TEMPORAL LOBECTOMY; WHITE MATTER; BRAIN CORTEX; CHROMOSOME 16; EPILEPSY; GENE DELETION; GENETICS; HIPPOCAMPUS; MUTATION; PATHOLOGY; TEMPORAL LOBE;

MICROTUBULE ASSOCIATED PROTEIN; NDE1 PROTEIN, HUMAN;

ADULT; CEREBRAL CORTEX; CHROMOSOMES, HUMAN, PAIR 16; EPILEPSY; EPILEPSY, TEMPORAL LOBE; FEMALE; HIPPOCAMPUS; HUMANS; MALE; MICROTUBULE-ASSOCIATED PROTEINS; MUTATION; SEQUENCE DELETION; TEMPORAL LOBE;

EID: 84859809937     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0034813     Document Type: Article

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