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Volumn 65, Issue 3, 1999, Pages 728-734

The gene for leukoencephalopathy with vanishing white matter is located on chromosome 3q27

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 3Q; ETHNIC GROUP; GENE LOCATION; GENE MAPPING; HAPLOTYPE; HUMAN; LEUKOENCEPHALOPATHY; MULTIGENE FAMILY; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; WHITE MATTER;

EID: 0033361759     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302548     Document Type: Article
Times cited : (75)

References (17)
  • 2
    • 0030695395 scopus 로고    scopus 로고
    • Oligodendrocyte-specific protein (OSP) is a major component of CNS myelin
    • Bronstein JM, Micevych PE, Chen K (1997) Oligodendrocyte-specific protein (OSP) is a major component of CNS myelin. J Neurosci Res 50:713-720
    • (1997) J Neurosci Res , vol.50 , pp. 713-720
    • Bronstein, J.M.1    Micevych, P.E.2    Chen, K.3
  • 3
    • 0029833675 scopus 로고    scopus 로고
    • Isolation and characterization of a novel oligodendrocyte-specific protein
    • Bronstein JM, Popper P, Micevych PE, Farber DB (1996b) Isolation and characterization of a novel oligodendrocyte-specific protein. Neurology 47:772-778
    • (1996) Neurology , vol.47 , pp. 772-778
    • Bronstein, J.M.1    Popper, P.2    Micevych, P.E.3    Farber, D.B.4
  • 4
    • 13344259999 scopus 로고    scopus 로고
    • A comprehensive generic map of the human genome based on 5,264 microsatellites
    • Dib C, Faure S, Fizames C, Samson D, Drouot N, Vignal A, Millasseau P, et al (1996) A comprehensive generic map of the human genome based on 5,264 microsatellites. Nature 380:152-154
    • (1996) Nature , vol.380 , pp. 152-154
    • Dib, C.1    Faure, S.2    Fizames, C.3    Samson, D.4    Drouot, N.5    Vignal, A.6    Millasseau, P.7
  • 5
    • 0027519635 scopus 로고
    • Diffuse white matter disease in three children: An encephalopathy with unique features on magnetic resonance imaging and proton magnetic resonance spectroscopy
    • Hanefeld F, Holzbach U, Kruse B, Wilichowsky E, Christen HJ, Frahm J (1993) Diffuse white matter disease in three children: an encephalopathy with unique features on magnetic resonance imaging and proton magnetic resonance spectroscopy. Neuropediatrics 24:244-248
    • (1993) Neuropediatrics , vol.24 , pp. 244-248
    • Hanefeld, F.1    Holzbach, U.2    Kruse, B.3    Wilichowsky, E.4    Christen, H.J.5    Frahm, J.6
  • 6
    • 0028857541 scopus 로고
    • Rapid multipoint linkage analysis of recessive traits in nuclear families, including homozygosity mapping
    • Kruglyak L, Daly MJ, Lander ES (1995) Rapid multipoint linkage analysis of recessive traits in nuclear families, including homozygosity mapping. Am J Hum Genet 56:519-527
    • (1995) Am J Hum Genet , vol.56 , pp. 519-527
    • Kruglyak, L.1    Daly, M.J.2    Lander, E.S.3
  • 8
    • 0027486810 scopus 로고
    • Déjérine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene
    • Roa BB, Dyck PJ, Marks HG, Chance PF, Lupski JR (1993a) Déjérine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene. Nat Genet 5:269-273
    • (1993) Nat Genet , vol.5 , pp. 269-273
    • Roa, B.B.1    Dyck, P.J.2    Marks, H.G.3    Chance, P.F.4    Lupski, J.R.5
  • 11
    • 0029078481 scopus 로고
    • Proton magnetic resonance spectroscopic imaging in childhood ataxia with diffuse central nervous system hypomyelination
    • Tedeschi G, Schiffmann R, Barton NW, Shih HH, Gospe SM Jr, Brady RO, Alger JR, et al (1995) Proton magnetic resonance spectroscopic imaging in childhood ataxia with diffuse central nervous system hypomyelination. Neurology 45:1526-1532
    • (1995) Neurology , vol.45 , pp. 1526-1532
    • Tedeschi, G.1    Schiffmann, R.2    Barton, N.W.3    Shih, H.H.4    Gospe S.M., Jr.5    Brady, R.O.6    Alger, J.R.7
  • 12
  • 16
    • 0025012109 scopus 로고
    • A bifunctional protein with deficient enzymic activity: Identification of a new peroxisomal disorder using novel methods to measure the peroxisomal beta-oxidation enzyme activities
    • Wanders RJ, van Roermund CW, Schelen A, Schutgens RB, Tager JM, Stephenson JB, Clayton PT (1990) A bifunctional protein with deficient enzymic activity: identification of a new peroxisomal disorder using novel methods to measure the peroxisomal beta-oxidation enzyme activities. J Inherit Metab Dis 13:375-379
    • (1990) J Inherit Metab Dis , vol.13 , pp. 375-379
    • Wanders, R.J.1    Van Roermund, C.W.2    Schelen, A.3    Schutgens, R.B.4    Tager, J.M.5    Stephenson, J.B.6    Clayton, P.T.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.