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[Incidence of A1555G mutations in the mitochondrial DNA and 35delG in the GJB2 gene (connexin-26) in families with late onset non-syndromic sensorineural hearing loss from Cantabria].
Gallo-Terán J, Morales-Angulo C, del Castillo I, Villamar M, Moreno-Pelayo MA, García-Mantilla J, Moreno F. Gallo-Terán J, et al. Among authors: moreno pelayo ma, moreno f. Acta Otorrinolaringol Esp. 2002 Oct;53(8):563-71. doi: 10.1016/s0001-6519(02)78349-0. Acta Otorrinolaringol Esp. 2002. PMID: 12530196 Free article. Spanish.
[Prevalence of the A1555G mutation in the mitochondrial DNA in patients with cochlear or vestibular damage due to aminoglycoside-induced ototoxicity].
Gallo-Terán J, Arellano B, Morales-Angulo C, Modamio-Høybjør S, Moreno-Pelayo MA, Ramírez-Camacho R, del Castillo I, Moreno F. Gallo-Terán J, et al. Among authors: moreno pelayo ma, moreno f. Acta Otorrinolaringol Esp. 2004 May;55(5):212-7. doi: 10.1016/s0001-6519(04)78511-8. Acta Otorrinolaringol Esp. 2004. PMID: 15461317 Free article. Spanish.
[Prevalence of the 35delG mutation in the GJB2 gene, del (GJB6-D13S1830) in the GJB6 gene, Q829X in the OTOF gene and A1555G in the mitochondrial 12S rRNA gene in subjects with non-syndromic sensorineural hearing impairment of congenital/childhood onset].
Gallo-Terán J, Morales-Angulo C, Rodríguez-Ballesteros M, Moreno-Pelayo MA, del Castillo I, Moreno F. Gallo-Terán J, et al. Among authors: moreno pelayo ma, moreno f. Acta Otorrinolaringol Esp. 2005 Dec;56(10):463-8. doi: 10.1016/s0001-6519(05)78649-0. Acta Otorrinolaringol Esp. 2005. PMID: 16425640 Free article. Spanish.
X-linked non-syndromic sensorineural deafness: the DFN6 locus.
del Castillo I, Rodríguez M, Cruz Tapia M, Moreno F. del Castillo I, et al. Among authors: moreno f. Adv Otorhinolaryngol. 2000;56:200-2. doi: 10.1159/000059100. Adv Otorhinolaryngol. 2000. PMID: 10868236 Review. No abstract available.
Molecular and clinical characterisation of three Spanish families with maternally inherited non-syndromic hearing loss caused by the 1494C->T mutation in the mitochondrial 12S rRNA gene.
Rodríguez-Ballesteros M, Olarte M, Aguirre LA, Galán F, Galán R, Vallejo LA, Navas C, Villamar M, Moreno-Pelayo MA, Moreno F, del Castillo I. Rodríguez-Ballesteros M, et al. Among authors: moreno pelayo ma, moreno f. J Med Genet. 2006 Nov;43(11):e54. doi: 10.1136/jmg.2006.042440. J Med Genet. 2006. PMID: 17085680 Free PMC article.
Heteroplasmy for the 1555A>G mutation in the mitochondrial 12S rRNA gene in six Spanish families with non-syndromic hearing loss.
del Castillo FJ, Rodríguez-Ballesteros M, Martín Y, Arellano B, Gallo-Terán J, Morales-Angulo C, Ramírez-Camacho R, Cruz Tapia M, Solanellas J, Martínez-Conde A, Villamar M, Moreno-Pelayo MA, Moreno F, del Castillo I. del Castillo FJ, et al. Among authors: moreno pelayo ma, moreno f. J Med Genet. 2003 Aug;40(8):632-6. doi: 10.1136/jmg.40.8.632. J Med Genet. 2003. PMID: 12920080 Free PMC article. No abstract available.
1,482 results