Arg133Cys mutation of Notch3 in two unrelated Japanese families with CADASIL

Internal Medicine

Volumn 39, Issue 9, 2000, Pages 732-737

  Uyama, Eiichiro ^a   Tokunaga, Makoto ^a   Suenaga, Akihito ^b   Kotorii, Satoru ^c   Kamimura, Kohei ^c   Takahashi, Keikichi ^c   Tabira, Takeshi ^c   Uchino, Makoto ^a  

^a KUMAMOTO UNIV SCHOOL OF MEDICINE   (Japan)

^b KITAKYUSHU CITY YAHATA HOSPITAL   (Japan)

^c NATIONAL INSTITUTE OF NEUROSCIENCE   (Japan)

Author keywords

Granular osmiophilic materials; Hereditary vascular dementia; Leukoaraiosis; Migraine; Multiple cerebral infarction

Indexed keywords

ARGININE; CELL SURFACE RECEPTOR; CYSTINE; NOTCH RECEPTOR; NOTCH3 PROTEIN, HUMAN; ONCOPROTEIN; PRIMER DNA;

ARTICLE; BRAIN; CASE REPORT; CHEMISTRY; DNA SEQUENCE; ETHNOLOGY; FEMALE; GENETICS; HUMAN; JAPAN; MALE; MIDDLE AGED; MULTIINFARCT DEMENTIA; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEOTIDE SEQUENCE; PATHOLOGY; PEDIGREE; POINT MUTATION; POLYMERASE CHAIN REACTION; SINGLE STRAND CONFORMATION POLYMORPHISM;

ARGININE; BRAIN; CYSTINE; DEMENTIA, MULTI-INFARCT; DNA MUTATIONAL ANALYSIS; DNA PRIMERS; FEMALE; HUMANS; JAPAN; MAGNETIC RESONANCE IMAGING; MALE; MIDDLE AGED; PEDIGREE; POINT MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; PROTO-ONCOGENE PROTEINS; RECEPTORS, CELL SURFACE; RECEPTORS, NOTCH; SEQUENCE ANALYSIS, DNA;

EID: 0034264344     PISSN: 09182918     EISSN: None     Source Type: Journal    
DOI: 10.2169/internalmedicine.39.732     Document Type: Article

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