Human doublecortin (DCX) and the homologous gene in mouse encode a putative Ca2+-dependent signaling protein which is mutated in human X-linked neuronal migration defects

Human Molecular Genetics

Volumn 7, Issue 8, 1998, Pages 1327-1332

  Sossey Alaoui, Khalid ^a   Hartung, Andrew J ^a   Guerrini, Renzo ^b   Manchester, David K ^c   Posar, Annio ^d   Puche Mira, A ^e   Andermann, Eva ^f   Dobyns, William B ^g   Srivastava, Anand K ^a  

^a GREENWOOD GENETIC CENTER   (United States)

^b UNIVERSITY OF PISA   (Italy)

^c CHILDREN S HOSPITAL   (United States)

^d UNIVERSITY OF BOLOGNA   (Italy)

^e HOSPITAL UNIVERSITARIO VIRGEN DE LA ARRIXACA   (Spain)

^f MCGILL UNIVERSITY   (Canada)

^g UNIV OF MINNESOTA HOSP AND CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM ION; MUTANT PROTEIN; SIGNAL PEPTIDE;

AGYRIA; ARTICLE; CELL MIGRATION; EPILEPSY; FRONTAL LOBE; GENE EXPRESSION; HETEROTOPIA; MENTAL DEFICIENCY; MISSENSE MUTATION; MOUSE; NERVE CELL; NONHUMAN; PRIORITY JOURNAL; TISSUE DISTRIBUTION; X CHROMOSOME LINKAGE;

EID: 0031829069     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/7.8.1327     Document Type: Article

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