Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

Nature

Volumn 383, Issue 6602, 1996, Pages 707-710

  Joutel, A ^a   Corpechot, C ^a   Ducros, A ^a   Vahedi, K ^a   Chabriat, H ^a   Mouton, P ^a   Alamowitch, S ^a   Domenga, V ^a   Cecillion, M ^a   Marechal, E ^a   Maciazek, J ^a   Vayssiere, C ^a   Cruaud, C ^a   Cabanis, E A ^a   Ruchoux, M M ^a   Weissanbach, J ^a   Bach, J F ^a   Bousser, M G ^a   Tournier Lasserve, E ^a  

^a INSERM   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BRAIN INFARCTION; BRAIN ISCHEMIA; CHROMOSOME 19; CLINICAL FEATURE; CONTROLLED STUDY; DEMENTIA; GENE DISRUPTION; GENE MAPPING; GENE MUTATION; HUMAN; LEUKOENCEPHALOPATHY; MAJOR CLINICAL STUDY; MULTIINFARCT DEMENTIA; ONSET AGE; PRIORITY JOURNAL; SIGNAL TRANSDUCTION; STROKE;

ADULT; AGE OF ONSET; AMINO ACID SEQUENCE; ANIMALS; CEREBRAL INFARCTION; CEREBROVASCULAR DISORDERS; CHROMOSOME MAPPING; CHROMOSOMES, ARTIFICIAL, YEAST; CHROMOSOMES, HUMAN, PAIR 19; DEMENTIA; DNA MUTATIONAL ANALYSIS; DROSOPHILA; HUMANS; MICE; MOLECULAR SEQUENCE DATA; MUTATION; PROTO-ONCOGENE PROTEINS; RECEPTORS, CELL SURFACE; RECEPTORS, NOTCH; SEQUENCE HOMOLOGY, AMINO ACID;

EID: 16044362074     PISSN: 00280836     EISSN: None     Source Type: Journal    
DOI: 10.1038/383707a0     Document Type: Article

References (0)