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Volumn 121, Issue 6, 2003, Pages 216-218

Familial susceptibility to aminoglycoside ototoxicity due to the A1555G mutation in the mitochondrial DNA;Predisposición familiar a la ototoxicidad de los aminoglucósidos debido a la mutación A1555G del ADN mitocondrial

Author keywords

A1555G; Aminoglycosides; Mitochondrial mutations; Nonsyndromic hearing loss; Ototoxicity

Indexed keywords

AMINOGLYCOSIDE ANTIBIOTIC AGENT; MITOCHONDRIAL DNA;

EID: 0042064951     PISSN: 00257753     EISSN: None     Source Type: Journal    
DOI: 10.1157/13049917     Document Type: Article
Times cited : (8)

References (10)
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  • 3
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    • Recomendación BIAP (Bureau International d'Audiophonologie) 02/1, Lisboa, Disponible en
    • Recomendación BIAP (Bureau International d'Audiophonologie) 02/1, Lisboa, 1997. Disponible en: http://www.biap.org
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    • Sarduy M, del Castillo I, Villamar M, Romero L, Herraiz C, Hernández FJ, et al. Genetic study of mitochondrially inherited sensorineural hearing impairment in eight large families from Spain and Cuba. In: Stephens D, Read A, Martini A, editors. Developments in genetic hearing impairment. London: Whurr Publishers, 1998; p. 121-5.
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  • 6
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    • The A1555G mutation in the 12S rRNA gene of human mtDNA: Recurrent origins and founder events in families affected by sensorineural deafness
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  • 7
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    • Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment with aminoglycosides
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.