A novel CNS gene required for neuronal migration and involved in X- linked subcortical laminar heterotopia and lissencephaly syndrome

Cell

Volumn 92, Issue 1, 1998, Pages 51-61

  Des Portes, Vincent ^a   Pinard, Jean Marc ^b   Billuart, Pierre ^a   Vinet, Marie Claude ^a   Koulakoff, Annette ^c   Carrié, Alain ^a   Gelot, Antoinette ^d   Dupuis, Elisabeth ^e   Motte, Jacques ^f   Berwald Netter, Yoheved ^c   Catala, Martin ^g   Kahn, Axel ^a   Beldjord, Cherif ^a   Chelly, Jamel ^a  

^a INSTITUT COCHIN   (France)

^b RAYMOND POINCARÉ HOSPITAL   (France)

^c l'alimentation et l'Environnement   (France)

^d HÔPITAL SAINT VINCENT DE PAUL   (France)

^e Service de Pédiatrie   (France)

^f AMERICAN MEMORIAL HOSPITAL   (France)

^g PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

BRAIN PROTEIN; DOUBLECORTIN; MUTANT PROTEIN; UNCLASSIFIED DRUG;

ADOLESCENT; AGYRIA; AMINO ACID SEQUENCE; AMINO TERMINAL SEQUENCE; ARTICLE; BRAIN DEVELOPMENT; CARBOXY TERMINAL SEQUENCE; CASE REPORT; CELL MIGRATION; CHILD; COGNITIVE DEFECT; EPILEPSY; FEMALE; GENE EXPRESSION; GENE MUTATION; GENETIC ANALYSIS; HETEROTOPIA; HUMAN; NERVE CELL; PRIORITY JOURNAL; PROTEIN DETERMINATION; SEQUENCE HOMOLOGY; SYNDROME; X CHROMOSOME LINKED DISORDER;

EID: 17444444915     PISSN: 00928674     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0092-8674(00)80898-3     Document Type: Article

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