000165972 001__ 165972
000165972 005__ 20260116163025.0
000165972 0247_ $$2doi$$a10.1136/jmg.39.12.e82
000165972 0248_ $$2sideral$$a117369
000165972 037__ $$aART-2002-117369
000165972 041__ $$aeng
000165972 100__ $$adel Castillo, F.
000165972 245__ $$aMaternally inherited non-syndromic hearing impairment in a Spanish family with the 7510T>C mutation in the mitochondrial tRNA(Ser(UCN)) gene.
000165972 260__ $$c2002
000165972 540__ $$9info:eu-repo/semantics/closedAccess$$aAll rights reserved$$uhttp://www.europeana.eu/rights/rr-f/
000165972 590__ $$a7.774$$b2002
000165972 591__ $$aGENETICS & HEREDITY$$b12 / 113 = 0.106$$c2002$$dQ1$$eT1
000165972 655_4 $$ainfo:eu-repo/semantics/article$$vinfo:eu-repo/semantics/publishedVersion
000165972 700__ $$aVillamar, M.
000165972 700__ $$aMoreno-Pelayo, M.
000165972 700__ $$aAlmela, J.
000165972 700__ $$aMorera, C.
000165972 700__ $$0(orcid)0000-0002-3265-504X$$aAdiego, I.$$uUniversidad de Zaragoza
000165972 700__ $$aMoreno, F.
000165972 700__ $$adel Castillo, I.
000165972 7102_ $$11004$$2653$$aUniversidad de Zaragoza$$bDpto. Cirugía,Ginecol.Obstetr.$$cÁrea Otorrinolaringología
000165972 773__ $$g39, 12 (2002), e82$$pJ. med. genet.$$tJOURNAL OF MEDICAL GENETICS$$x0022-2593
000165972 8564_ $$s271687$$uhttps://zaguan.unizar.es/record/165972/files/texto_completo.pdf$$yVersión publicada
000165972 8564_ $$s2350960$$uhttps://zaguan.unizar.es/record/165972/files/texto_completo.jpg?subformat=icon$$xicon$$yVersión publicada
000165972 909CO $$ooai:zaguan.unizar.es:165972$$particulos$$pdriver
000165972 951__ $$a2026-01-16-14:53:58
000165972 980__ $$aARTICLE