CADASIL syndrome in a large Turkish kindred caused by the R90C mutation in the Notch3 receptor

European Journal of Neurology

Volumn 9, Issue 1, 2002, Pages 23-28

  Utku, U ^a   Celik, Y ^a   Uyguner, O ^b   Yuksel Apak M ^b   Wollnik, B ^b  

^a TRAKYA UNIVERSITY   (Turkey)

^b ISTANBUL UNIVERSITY   (Turkey)

Author keywords

CADASIL syndrome; Clinical evaluation; Migraine; Mutation screening; Notch3 receptor

Indexed keywords

NOTCH RECEPTOR; RECEPTOR;

ADULT; AMINO TERMINAL SEQUENCE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CADASIL; CASE REPORT; CLINICAL FEATURE; CONTROLLED STUDY; DIAGNOSTIC ACCURACY; FAMILY; FEMALE; GENE MUTATION; HETEROZYGOTE; HUMAN; MIGRAINE; MOLECULAR BIOLOGY; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; RECURRENT DISEASE; STROKE; TURKEY (REPUBLIC);

BRAIN; CEREBROVASCULAR ACCIDENT; DEMENTIA, MULTI-INFARCT; DNA MUTATIONAL ANALYSIS; EXONS; FEMALE; HUMANS; MAGNETIC RESONANCE IMAGING; MIDDLE AGED; MUTATION; PEDIGREE; PROTO-ONCOGENE PROTEINS; RECEPTORS, CELL SURFACE; RECEPTORS, NOTCH; TOMOGRAPHY, X-RAY COMPUTED; TURKEY;

EID: 0036393522     PISSN: 13515101     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1468-1331.2002.00344.x     Document Type: Article

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