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Volumn 59, Issue 6, 1996, Pages 1210-1220

Human peroxisome assembly factor-2 (PAF-2): A gene responsible for group C peroxisome biogenesis disorder in humans

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; COMPLEMENTARY DNA; DNA; MESSENGER RNA; NUCLEOTIDE;

EID: 19244362560     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (96)

References (5)
  • 1
    • 0025876501 scopus 로고
    • Identification of RNA splicing errors resulting in human ornithine transcarbamylase deficiency
    • Carstens RP, Fenton WA, Rosenberg LR (1991) Identification of RNA splicing errors resulting in human ornithine transcarbamylase deficiency. Am J Hum Genet 48:1105-1114
    • (1991) Am J Hum Genet , vol.48 , pp. 1105-1114
    • Carstens, R.P.1    Fenton, W.A.2    Rosenberg, L.R.3
  • 3
    • 0028817372 scopus 로고
    • Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders
    • Dodt G, Braverman NC, Moser A, Moser W, Watkins P, Valle D, Gould SJ (1995) Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders. Nat Genet 9:115-125
    • (1995) Nat Genet , vol.9 , pp. 115-125
    • Dodt, G.1    Braverman, N.C.2    Moser, A.3    Moser, W.4    Watkins, P.5    Valle, D.6    Gould, S.J.7
  • 4
    • 0023577538 scopus 로고
    • Human adenine phosphoribosyltransferase: Identification of allelic mutations at the nucleotide level as a cause of complete deficiency of the enzyme
    • Hidaka Y, Palella TD, O'Tool TE, Tarle SA, Kelley WN (1987) Human adenine phosphoribosyltransferase: identification of allelic mutations at the nucleotide level as a cause of complete deficiency of the enzyme. J Clin Invest 80:1409-1415
    • (1987) J Clin Invest , vol.80 , pp. 1409-1415
    • Hidaka, Y.1    Palella, T.D.2    O'Tool, T.E.3    Tarle, S.A.4    Kelley, W.N.5
  • 5
    • 0025083351 scopus 로고
    • Regional assignment of the human thymidylate synthase (TS) gene to chromosome band 18p11.32 by non-isotopic in situ hybridization
    • Hori T, Takahashi E, Ayusawa D, Takeishi K, Kaneda S, Seno T (1990) Regional assignment of the human thymidylate synthase (TS) gene to chromosome band 18p11.32 by non-isotopic in situ hybridization. Hum Genet 85:576-580
    • (1990) Hum Genet , vol.85 , pp. 576-580
    • Hori, T.1    Takahashi, E.2    Ayusawa, D.3    Takeishi, K.4    Kaneda, S.5    Seno, T.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.