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American Journal of Human Genetics
Volumn 58, Issue 3, 1996, Pages 506-512
The age of human mutation: Genealogical and linkage disequilibrium analysis of the CLN5 mutation in the Finnish population
Author keywords

[No Author keywords available]
Indexed keywords

ALLELE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 13Q; CLINICAL ARTICLE; CONTROLLED STUDY; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENE MUTATION; GENEALOGY; HAPLOTYPE; HUMAN; LIPOFUSCINOSIS; METABOLIC ENCEPHALOPATHY; PEDIGREE ANALYSIS; PRIORITY JOURNAL;
EID: 0030028560     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (59)
References (5)
  • 1
    • 0027448693 scopus 로고
    • Familial Mediterranean fever (FMF) in Moroccan Jews: Demonstration of a founder effect by extended haplotype analysis
    • Aksentijevich I, Pras E, Gruberg L, Shen Y, Holman K, Helling S, Prosen I, et al (1993) Familial Mediterranean fever (FMF) in Moroccan Jews: demonstration of a founder effect by extended haplotype analysis. Am J Hum Genet 53:644-651
    • (1993) Am J Hum Genet , vol.53 , pp. 644-651
    • Aksentijevich, I.1    Pras, E.2    Gruberg, L.3    Shen, Y.4    Holman, K.5    Helling, S.6    Prosen, I.7
  • 3
    • 0026949420 scopus 로고
    • Linkage disequilibrium mapping in isolated founder populations: Diastrophic dysplasia in Finland
    • Hästbacka J, de la Chapelle A, Kaitila I, Sistonen P, Weaver A, Lander E (1992) Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland. Nat Genet 2:204-211
    • (1992) Nat Genet , vol.2 , pp. 204-211
    • Hästbacka, J.1    De La Chapelle, A.2    Kaitila, I.3    Sistonen, P.4    Weaver, A.5    Lander, E.6
  • 4
    • 0027315230 scopus 로고
    • Refined assignment of the infantile neuronal ceroid lipofuscinosis (INCL, CLN1) locus at 1p32: Incorporation of linkage disequilibrium in multipoint analysis
    • Hellsten E, Vesa J, Speer M, Mäkelä TP, Järvelä I, Alitalo K, Ott J, et al (1993) Refined assignment of the infantile neuronal ceroid lipofuscinosis (INCL, CLN1) locus at 1p32: incorporation of linkage disequilibrium in multipoint analysis. Genomics 16:720-725
    • (1993) Genomics , vol.16 , pp. 720-725
    • Hellsten, E.1    Vesa, J.2    Speer, M.3    Mäkelä, T.P.4    Järvelä, I.5    Alitalo, K.6    Ott, J.7
  • 5
    • 0028345785 scopus 로고
    • Northern epilepsy syndrome: An inherited childhood epilepsy with associated mental retardation
    • Hirvasniemi A, Lang H, Lehesjoki A-E, Leisti J (1994) Northern epilepsy syndrome: an inherited childhood epilepsy with associated mental retardation. J Med Genet 31:177-182
    • (1994) J Med Genet , vol.31 , pp. 177-182
    • Hirvasniemi, A.1    Lang, H.2    Lehesjoki, A.-E.3    Leisti, J.4

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.