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Volumn 43, Issue 2, 1997, Pages 149-155

Determination of the genomic structure of the XNP/ATRX gene encoding a potential zinc finger helicase

Author keywords

[No Author keywords available]

Indexed keywords

HELICASE; ZINC FINGER PROTEIN;

EID: 0031571118     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1997.4793     Document Type: Article
Times cited : (60)

References (15)
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    • Gecz, J., Polard, H., Consalez, G., Villard, L., Stayton, C., Millasseau, P., Khrestchatisky, M., and Fontes, M. (1994). Cloning and expression of the murine homologue of a putative human X-linked nuclear protein gene closely linked to PGK1 (Xq13.3). Hum. Mol. Genet. 3: 39-44.
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  • 4
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    • Mutations in a putative global transcriptional regulator cause X-linked mental retardation with a-thalassemia (ATR-X syndrome)
    • Gibbons, R. J., Picketts, D. J., Villard, L., and Higgs, D. R. (1995). Mutations in a putative global transcriptional regulator cause X-linked mental retardation with a-thalassemia (ATR-X syndrome). Cell 80: 837-845.
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  • 5
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    • A novel mutation in the putative DNA helicase XH2 is responsible for male-to-female sex reversal associated with an atypical form of the ATR-X syndrome
    • Ion, A., Telvi, L., Chaussain, J. L., Galacteros, F., Valayer, J., Fellous, M., and McElreavey, K. (1996). A novel mutation in the putative DNA helicase XH2 is responsible for male-to-female sex reversal associated with an atypical form of the ATR-X syndrome. Am. J. Hum. Genet. 58: 1185-1191.
    • (1996) Am. J. Hum. Genet. , vol.58 , pp. 1185-1191
    • Ion, A.1    Telvi, L.2    Chaussain, J.L.3    Galacteros, F.4    Valayer, J.5    Fellous, M.6    McElreavey, K.7
  • 6
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    • Compilation and analysis of sequences upstream from the translational start site in eukaryotic mRNAs
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    • The mutational spectrum of single base-pair substitutions in mRNA splice junctions of human genes: Causes and consequences
    • Krawczak, M., Reiss, J., and Cooper, D. N. (1992). The mutational spectrum of single base-pair substitutions in mRNA splice junctions of human genes: Causes and consequences. Hum. Genet. 90: 41-50.
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    • Krawczak, M.1    Reiss, J.2    Cooper, D.N.3
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    • Splicing mutation in the ATR-X gene can lead to a dysmorphic mental retardation phenotype without a-thalassemia
    • Villard, L., Toutain, A., Lossi, A. M., Gecz, J., Houdayer, C., Moraine, C., and Fontès, M. (1996a). Splicing mutation in the ATR-X gene can lead to a dysmorphic mental retardation phenotype without a-thalassemia. Am. J. Hum. Genet. 58: 499-505.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.