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Volumn 32, Issue 1, 1996, Pages 151-154

Identification of a key recombinant narrows the CADASIL gene region to 8 cM and argues against allelism of CADASIL and familial hemiplegic migraine

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

EID: 0029932262     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.0094     Document Type: Article
Times cited : (25)

References (11)
  • 1
    • 0028156770 scopus 로고
    • Summary of the proceedings of the first international workshop on CADASIL, Paris, May 19-21, 1993
    • Bousser, M. G., and Tournier-Lasserve, E. (1994). Summary of the proceedings of the first international workshop on CADASIL, Paris, May 19-21, 1993. Stroke 25: 704-707.
    • (1994) Stroke , vol.25 , pp. 704-707
    • Bousser, M.G.1    Tournier-Lasserve, E.2
  • 2
    • 0012688996 scopus 로고
    • Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): Main clinical findings in five families
    • Chabriat, H., Tournier-Lasserve, E., and Nibbio, A. (1994). Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): Main clinical findings in five families. Stroke 25: 258.
    • (1994) Stroke , vol.25 , pp. 258
    • Chabriat, H.1    Tournier-Lasserve, E.2    Nibbio, A.3
  • 8
    • 0023275907 scopus 로고
    • Mendelian etiologies of stroke
    • Natowitz, M., and Kelley, R. I. (1987). Mendelian etiologies of stroke. Ann. Neurol. 22: 175-192.
    • (1987) Ann. Neurol. , vol.22 , pp. 175-192
    • Natowitz, M.1    Kelley, R.I.2
  • 9
    • 0028943944 scopus 로고
    • Cerebral autosomal dominant arteriopathy with infarcts and leucoencephalopathy (CADASIL). Clinical, neuroimaging, pathological and genetic study of a large italian family
    • Sabbadini, G., Francia, A., Calandriello, L., Di Biasi, C., Trasimeni, G., Gualdi, G. F., Palladini, G., Manfredi, M., and Frontali, M. (1995). Cerebral autosomal dominant arteriopathy with infarcts and leucoencephalopathy (CADASIL). Clinical, neuroimaging, pathological and genetic study of a large Italian family. Brain 118: 207-215.
    • (1995) Brain , vol.118 , pp. 207-215
    • Sabbadini, G.1    Francia, A.2    Calandriello, L.3    Di Biasi, C.4    Trasimeni, G.5    Gualdi, G.F.6    Palladini, G.7    Manfredi, M.8    Frontali, M.9
  • 10
    • 0028986010 scopus 로고
    • Hereditary multi-infarct dementia unlinked to chromosome 19q12 in a large Scottish pedigree: Evidence of probable locus heterogeneity
    • St. Clair, D., Bolt, J., Morris, S., and Doyle, D. (1995). Hereditary multi-infarct dementia unlinked to chromosome 19q12 in a large Scottish pedigree: Evidence of probable locus heterogeneity. J. Med. Genet. 32: 57-60.
    • (1995) J. Med. Genet. , vol.32 , pp. 57-60
    • St Clair, D.1    Bolt, J.2    Morris, S.3    Doyle, D.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.