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Volumn 63, Issue 4, 1998, Pages 1078-1085

Assignment of the locus for congenital lactase deficiency to 2q21, in the vicinity of but separate from the lactase-phlorizin hydrolase gene

Author keywords

[No Author keywords available]

Indexed keywords

HYDROLASE; LACTASE; PHLORIZIN;

EID: 1642586712     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302064     Document Type: Article
Times cited : (70)

References (24)
  • 1
    • 0026321407 scopus 로고
    • Statistical methods for multipoint radiation hybrid mapping
    • Boehnke M, Lange K, Cox DR (1991) Statistical methods for multipoint radiation hybrid mapping. Am J Hum Genet 49: 1174-1188
    • (1991) Am J Hum Genet , vol.49 , pp. 1174-1188
    • Boehnke, M.1    Lange, K.2    Cox, D.R.3
  • 2
    • 0025882118 scopus 로고
    • Structure of the chromosomal gene and cDNAs coding for lactase-phlorizin hydrolase in humans with adult-type hypolactasia or persistence of lactose
    • Boll W, Wagner P, Mantei N (1991) Structure of the chromosomal gene and cDNAs coding for lactase-phlorizin hydrolase in humans with adult-type hypolactasia or persistence of lactose. Am J Hum Genet 48:889-902
    • (1991) Am J Hum Genet , vol.48 , pp. 889-902
    • Boll, W.1    Wagner, P.2    Mantei, N.3
  • 4
    • 0025131820 scopus 로고
    • Radiation hybrid mapping: A somatic cell genetic method for constructing high-resolution map of mammalian chromosomes
    • Cox DR, Burmeister M, Price ER, Kim S, Myers RM (1990) Radiation hybrid mapping: a somatic cell genetic method for constructing high-resolution map of mammalian chromosomes. Science 250:245-250
    • (1990) Science , vol.250 , pp. 245-250
    • Cox, D.R.1    Burmeister, M.2    Price, E.R.3    Kim, S.4    Myers, R.M.5
  • 5
    • 13344259999 scopus 로고    scopus 로고
    • A comprehensive genetic map of the human genome based on 5,264 microsatellites
    • Dib C, Fauré S, Fizames C, Samson D, Drouot N, Vignal A, Millasseau P, et al (1996) A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 380:152-154
    • (1996) Nature , vol.380 , pp. 152-154
    • Dib, C.1    Fauré, S.2    Fizames, C.3    Samson, D.4    Drouot, N.5    Vignal, A.6    Millasseau, P.7
  • 6
    • 0027421312 scopus 로고
    • Regional localization of the lactase-phlorizin hydrolase gene, LCT, to chromosome 2q21
    • Harvey CB, Fox MF, Jeggo PA, Mantei N, Povey S, Swallow DM (1993) Regional localization of the lactase-phlorizin hydrolase gene, LCT, to chromosome 2q21. Ann Hum Genet 57:179-185
    • (1993) Ann Hum Genet , vol.57 , pp. 179-185
    • Harvey, C.B.1    Fox, M.F.2    Jeggo, P.A.3    Mantei, N.4    Povey, S.5    Swallow, D.M.6
  • 7
    • 0001036207 scopus 로고
    • Defective lactose absorption causing malnutrition in infancy
    • Holzel A, Schwarz V, Sutcliffe KW (1959) Defective lactose absorption causing malnutrition in infancy. Lancet i: 1126-1128
    • (1959) Lancet , vol.1 , pp. 1126-1128
    • Holzel, A.1    Schwarz, V.2    Sutcliffe, K.W.3
  • 11
    • 0024076253 scopus 로고
    • Complete primary structure of human and rabbit lactase-phlorizin hydrolase: Implications for biosynthesis, membrane anchoring and evolution of the enzyme
    • Mantei N, Villa M, Enzler T, Wacker H, Boll W, James P, Hunziker W, et al (1988) Complete primary structure of human and rabbit lactase-phlorizin hydrolase: implications for biosynthesis, membrane anchoring and evolution of the enzyme. EMBO J 7:2705-2713
    • (1988) EMBO J , vol.7 , pp. 2705-2713
    • Mantei, N.1    Villa, M.2    Enzler, T.3    Wacker, H.4    Boll, W.5    James, P.6    Hunziker, W.7
  • 12
    • 0015436884 scopus 로고
    • The Finnish population structure
    • Nevanlinna H (1972) The Finnish population structure. Hereditas 71:195-236
    • (1972) Hereditas , vol.71 , pp. 195-236
    • Nevanlinna, H.1
  • 13
    • 0028071914 scopus 로고
    • Infantile onset spinocerebellar ataxia represents an allelic disease distinct from other hereditary ataxias
    • Nikali K, Koskinen T, Suomalainen A, Pihko H, Peltonen L (1994) Infantile onset spinocerebellar ataxia represents an allelic disease distinct from other hereditary ataxias. Pediatr Res 36:607-612
    • (1994) Pediatr Res , vol.36 , pp. 607-612
    • Nikali, K.1    Koskinen, T.2    Suomalainen, A.3    Pihko, H.4    Peltonen, L.5
  • 15
    • 0030954650 scopus 로고    scopus 로고
    • Rare disease genes: Lessons and challenges
    • Peltonen L, Uusitalo A (1997) Rare disease genes: lessons and challenges. Genome Res 7:765-767
    • (1997) Genome Res , vol.7 , pp. 765-767
    • Peltonen, L.1    Uusitalo, A.2
  • 16
    • 1642608680 scopus 로고
    • Molecular analysis of the lactase gene in the congenital lactase deficiency
    • Poggi V, Sebastio G (1991) Molecular analysis of the lactase gene in the congenital lactase deficiency. Am J Hum Genet Suppl 49:105
    • (1991) Am J Hum Genet Suppl , vol.49 , pp. 105
    • Poggi, V.1    Sebastio, G.2
  • 20
    • 0028968329 scopus 로고
    • A powerful likelihood method for the analysis of linkage disequilibrium between trait loci and one or more polymorphic marker loci
    • Terwilliger JD (1995) A powerful likelihood method for the analysis of linkage disequilibrium between trait loci and one or more polymorphic marker loci. Am J Hum Genet 56: 777-787
    • (1995) Am J Hum Genet , vol.56 , pp. 777-787
    • Terwilliger, J.D.1
  • 21
    • 0038854380 scopus 로고    scopus 로고
    • Reply to Sham et al
    • _ (1996) Reply to Sham et al. Am J Hum Genet 58: 1095-1096
    • (1996) Am J Hum Genet , vol.58 , pp. 1095-1096
  • 23
    • 0029812169 scopus 로고    scopus 로고
    • Tracing an ancestral mutation: Genealogical and haplotype analysis of the infantile onset spinocerebellar ataxia locus
    • Varilo T, Nikali K, Suomalainen A, Lönnqvist T, Peltonen L (1996a) Tracing an ancestral mutation: genealogical and haplotype analysis of the infantile onset spinocerebellar ataxia locus. Genome Res 6:870-875
    • (1996) Genome Res , vol.6 , pp. 870-875
    • Varilo, T.1    Nikali, K.2    Suomalainen, A.3    Lönnqvist, T.4    Peltonen, L.5
  • 24
    • 0030028560 scopus 로고    scopus 로고
    • The age of human mutation: Genealogical and linkage disequilibrium analysis of the CLN5 mutation in the Finnish population
    • Varilo T, Savukoski M, Norio R, Santavuori P, Peltonen L, Järvelä I (1996b) The age of human mutation: genealogical and linkage disequilibrium analysis of the CLN5 mutation in the Finnish population. Am J Hum Genet 58:506-512
    • (1996) Am J Hum Genet , vol.58 , pp. 506-512
    • Varilo, T.1    Savukoski, M.2    Norio, R.3    Santavuori, P.4    Peltonen, L.5    Järvelä, I.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.