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Volumn 11, Issue 9, 1997, Pages 553-554

Genetics of stroke

Author keywords

Cerebrovascular; Genetics; Stroke

Indexed keywords

ANIMAL MODEL; CHROMOSOME; GENETICS; HUMAN; NONHUMAN; PHENOTYPE; SHORT SURVEY; STROKE;

EID: 0030688989     PISSN: 09509240     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.jhh.1000486     Document Type: Short Survey
Times cited : (1)

References (12)
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    • Cerebral autosomal dominant art-eriopathy with subcortical infarcts and leukencephalopathy maps to chromosome 19q12
    • Tournier-Lasserve. Cerebral autosomal dominant art-eriopathy with subcortical infarcts and leukencephalopathy maps to chromosome 19q12. Nat Genet 1993; 3: 256-259.
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    • Notch 3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia
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    • Kobayashi Y et al. Respiration-deficient cells are caused by a single point mutation in the mitochondrial tRNA-Leu (VUR) gene in mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS). Am J Hum Genet 1991; 49: 590-599.
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    • Kobayashi, Y.1
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    • Counting strokes - News and views
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    • Chromosomal mapping of quantitative trait loci contributing to stroke in a rat model of complex human disease
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    • Sensitivity to cerebral ischaemic insult in a rat model of stroke is determined by a single genetic locus: Possible analogy to human ischaemic stroke
    • in press
    • Jeffs B et al. Sensitivity to cerebral ischaemic insult in a rat model of stroke is determined by a single genetic locus: possible analogy to human ischaemic stroke. Nat Genet (in press).
    • Nat Genet
    • Jeffs, B.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.