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Volumn 21, Issue 6, 2005, Pages 312-314

Nuclear genes and mitochondrial translation: A new class of genetic disease

Author keywords

[No Author keywords available]

Indexed keywords

GENE MUTATION; GENETIC CODE; GENETIC DISORDER; GENETIC IDENTIFICATION; HUMAN; MITOCHONDRION; NONHUMAN; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN SYNTHESIS; RNA TRANSLATION; SHORT SURVEY;

EID: 19444380425     PISSN: 01689525     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tig.2005.04.003     Document Type: Short Survey
Times cited : (110)

References (13)
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  • 5
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    • Yasukawa, T.1
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    • Y. Kirino Codon-specific translational defect caused by a wobble modification deficiency in mutant tRNA from a human mitochondrial disease Proc. Natl. Acad. Sci. U. S. A. 101 2004 15070 15075
    • (2004) Proc. Natl. Acad. Sci. U. S. A. , vol.101 , pp. 15070-15075
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    • Missense mutation in pseudouridine synthase 1 (PUS1) causes mitochondrial myopathy and sideroblastic anemia (MLASA)
    • Y. Bykhovskaya Missense mutation in pseudouridine synthase 1 (PUS1) causes mitochondrial myopathy and sideroblastic anemia (MLASA) Am. J. Hum. Genet. 74 2004 1303 1308
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.