Genetic malformations of cortical development

Experimental Brain Research

Volumn 173, Issue 2, 2006, Pages 322-333

  Guerrini, Renzo ^a   Marini, Carla ^a  

^a DEPARTMENT OF DEVELOPMENTAL NEUROSCIENCE   (Italy)

Author keywords

Cortical malformations; Epilepsy; Genetics; Lissencephaly; Periventricular nodular heterotopia; Polymicrogyria

Indexed keywords

DOUBLECORTIN; REELIN;

ARGEF2 GENE; ARX GENE; AUTOSOMAL DOMINANT INHERITANCE; AUTOSOMAL RECESSIVE DISORDER; BRAIN CORTEX; BRAIN DEVELOPMENT; BRAIN MALFORMATION; BRAIN REGION; CELL MIGRATION; CEREBELLUM HYPOPLASIA; CHROMOSOME 22Q; CHROMOSOME DELETION; CHROMOSOME XQ; CHROMOSOME XQ28; CONFERENCE PAPER; CONGENITAL MALFORMATION; CORPUS CALLOSUM AGENESIS; DCX GENE; DEVELOPMENTAL DISORDER; ELECTROENCEPHALOGRAM; FAMILIAL DISEASE; FEMALE; FLNA GENE; FOCAL EPILEPSY; GENE; GENE MUTATION; GENETIC DISORDER; GENETIC HETEROGENEITY; GENETIC LINKAGE; GENOTYPE; GPR56 GENE; HETEROTOPIA; HUMAN; IN VIVO STUDY; INFANTILE SPASM; LIS1 GENE; MALE; MICROCEPHALY; MICROGYRIA; MUSCLE HYPOTONIA; NERVE CELL; NERVE CELL DEGENERATION; NONHUMAN; NUCLEAR MAGNETIC RESONANCE IMAGING; PACHYGYRIA; PATHOPHYSIOLOGY; PERIVENTRICULAR NODULAR HETEROTOPIA; PHENOTYPE; PRIORITY JOURNAL; RECESSIVE GENE; RECESSIVE INHERITANCE; RELN GENE; SEIZURE; SEX RATIO; X CHROMOSOME LINKED DISORDER;

CEREBRAL CORTEX; EPILEPSY; HUMANS; MUTATION;

EID: 33747594579     PISSN: 00144819     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00221-006-0501-z     Document Type: Conference Paper

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