Mutations of the Notch3 gene in non-Caucasian patients with suspected CADASIL syndrome

Dementia and Geriatric Cognitive Disorders

Volumn 12, Issue 3, 2001, Pages 185-193

  Kotorii, Satoshi ^a   Takahashi, Keikichi ^a   Kamimura, Kohei ^a   Nishio, Takeshi ^b   Arima, Kunimasa ^c,d   Yamada, Haruki ^e   Uyama, Eiichiro ^f   Uchino, Makoto ^f   Suenaga, Akihito ^g   Matsumoto, Masayasu ^h   Kuchel, George ⁱ   Rouleau, Guy A ⁱ   Tabira, Takeshi ^a  

^a NATIONAL INSTITUTE OF NEUROSCIENCE   (Japan)

^b National Center of Neurology and Psychiatry   (Japan)

^c NATIONAL INSTITUTE OF MENTAL HEALTH   (Japan)

^d TOKYO METROPOLITAN INSTITUTE OF MEDICAL SCIENCE   (Japan)

^e KAWASAKI MEDICAL SCHOOL   (Japan)

^f KUMAMOTO UNIV SCHOOL OF MEDICINE   (Japan)

^g Saiseikai Yahata Hospital   (Japan)

^h OSAKA UNIVERSITY MEDICAL SCHOOL   (Japan)

ⁱ MONTREAL GENERAL HOSPITAL   (Canada)

Author keywords

CADASIL; Leukoencephalopathy; Notch3; Stroke; Vascular dementia

Indexed keywords

CYSTEINE; NOTCH RECEPTOR;

ADULT; AGED; AMINO ACID SUBSTITUTION; ARTERY DISEASE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BRAIN INFARCTION; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DNA POLYMORPHISM; EXON; FAMILY HISTORY; FEMALE; GENE MUTATION; GENE SEQUENCE; GENETIC PREDISPOSITION; HUMAN; LEUKOENCEPHALOPATHY; MALE; MISSENSE MUTATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PEDIGREE; PRIORITY JOURNAL; RACE DIFFERENCE; SEQUENCE ANALYSIS;

ADULT; AGED; DEMENTIA, MULTI-INFARCT; DNA FRAGMENTATION; DNA MUTATIONAL ANALYSIS; DNA PRIMERS; EXONS; FEMALE; HUMANS; JAPAN; MALE; MIDDLE AGED; MUTATION, MISSENSE; PEDIGREE; POINT MUTATION; POLYMERASE CHAIN REACTION; PROTO-ONCOGENE PROTEINS; RECEPTORS, CELL SURFACE; RECEPTORS, NOTCH; SEQUENCE ANALYSIS, DNA; SILOXANES;

EID: 17744369485     PISSN: 14208008     EISSN: None     Source Type: Journal    
DOI: 10.1159/000051256     Document Type: Article

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