Identification of a Notch3 mutation in a Japanese CADASIL family

Alzheimer Disease and Associated Disorders

Volumn 13, Issue 4, 1999, Pages 222-225

  Kamimura, Kohei ^a   Takahashi, Keikichi ^a   Uyama, Eiichiro ^b   Tokunaga, Makoto ^b   Kotorii, Satoshi ^a   Uchino, Makoto ^b   Tabira, Takeshi ^a  

^a NATIONAL INSTITUTE OF NEUROSCIENCE   (Japan)

^b KUMAMOTO UNIV SCHOOL OF MEDICINE   (Japan)

Author keywords

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL); Hereditary multi infarct dimentia; Missense mutation; Notch3 gene

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BRAIN INFARCTION; CASE REPORT; CAUCASIAN; CEREBROVASCULAR DISEASE; CHROMOSOME 19; DEMENTIA; FACIAL NERVE PARALYSIS; FEMALE; GENE MUTATION; GENETIC ANALYSIS; HUMAN; JAPAN; LEUKOENCEPHALOPATHY; MALE; MISSENSE MUTATION; PRIORITY JOURNAL; RECURRENT DISEASE; STROKE; SYNDROME CADASIL;

EID: 0033429146     PISSN: 08930341     EISSN: None     Source Type: Journal    
DOI: 10.1097/00002093-199910000-00008     Document Type: Article

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