A locus for bilateral occipital polymicrogyria maps to chromosome 6q16-q22

Neurogenetics

Volumn 10, Issue 1, 2009, Pages 35-42

  Ouled Amar Ben Cheikh, Bouchra ^a,b,c   Baulac, Stéphanie ^a,b   Lahjouji, Fatiha ^c   Bouhouche, Ahmed ^c   Couarch, Philippe ^a,b   Khalili, Naima ^c   Regragui, Wafae ^c   Lehericy, Stéphane ^d   Ruberg, Merle ^a,b   Benomar, Ali ^c   Heath, Simon ^e   Chkili, Taib ^f   Yahyaoui, Mohamed ^c   Jiddane, Mohamed ^c   Ouazzani, Reda ^c   Leguern, Eric ^d  

^a INSERM   (France)

^b SORBONNE UNIVERSITÉ   (France)

^c IBN SINA HOSPITAL   (Morocco)

^d PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^e CENTRE NATIONAL DE GÉNOTYPAGE   (France)

^f MOHAMMED V UNIVERSITY   (Morocco)

Author keywords

Chromosome 6q16 q22; Epilepsy; Homozygosity mapping; Polymicrogyria; Psychosis

Indexed keywords

CELL NUCLEUS RECEPTOR; G PROTEIN COUPLED RECEPTOR; GLUTAMATE RECEPTOR; MARCKS PROTEIN; PROTEIN GPR6; PROTEIN GPRC6A; PROTEIN GRIK2; PROTEIN MICAL1; PROTEIN NR2E1; PROTEIN TUBE1; SIGNAL PEPTIDE; TUBULIN; UNCLASSIFIED DRUG;

ABNORMAL BEHAVIOR; ADULT; ARTICLE; CHROMOSOME 6Q; CLINICAL ARTICLE; COMPLEX PARTIAL SEIZURE; CONTROLLED STUDY; FEMALE; GENE FUNCTION; GENE LOCUS; GENE MUTATION; HOMOZYGOSITY; HUMAN; MALE; MICROGYRIA; NUCLEAR MAGNETIC RESONANCE IMAGING; OCCIPITAL LOBE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

ADULT; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 6; CONSANGUINITY; DNA MUTATIONAL ANALYSIS; FAMILY; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; LOD SCORE; MAGNETIC RESONANCE IMAGING; MALE; MALFORMATIONS OF CORTICAL DEVELOPMENT; MIDDLE AGED; MOROCCO; POLYMORPHISM, SINGLE NUCLEOTIDE; YOUNG ADULT;

EID: 58649124725     PISSN: 13646745     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10048-008-0143-3     Document Type: Article

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