Normal view MARC view ISBD view

Andrade, Danielle M

Genetic basis in epilepsies caused by malformations of cortical development and in those with structurally normal brain. [electronic resource] - Human genetics Jul 2009 - 173-93 p. digital

Publication Type: Comparative Study; Journal Article; Review

ISSN: 1432-1203

Standard No.: 10.1007/s00439-009-0702-1 doi

Subjects--Topical Terms:
ADAM Proteins--genetics
ADAMTS4 Protein
Brain--anatomy & histology
Cathepsin B--genetics
Cerebral Cortex--abnormalities
Child, Preschool
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 22
Chromosomes, Human, Pair 3
Classical Lissencephalies and Subcortical Band Heterotopias--complications
Collagen Type XVIII
Epilepsy--etiology
Eye Proteins--genetics
Homeodomain Proteins--genetics
Humans
Lissencephaly--complications
Male
Malformations of Cortical Development--complications
Membrane Proteins
Mutation
Neoplasm Proteins
Nerve Tissue Proteins--genetics
PAX6 Transcription Factor
Paired Box Transcription Factors--genetics
Periventricular Nodular Heterotopia--complications
Procollagen N-Endopeptidase--genetics
Radiography
Receptors, G-Protein-Coupled--genetics
Repressor Proteins--genetics
T-Box Domain Proteins--genetics
Transcription Factors--genetics