A novel deletion involving the connexin-30 gene, del(GJB6- d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment

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dc.contributor.authordel Castillo, F. J.
dc.contributor.authorRodríguez Ballesteros, M.
dc.contributor.authorÁlvarez, A.
dc.contributor.authorHutchin, T.
dc.contributor.authorLeonardi, E.
dc.contributor.authorde Oliveira, C. A.
dc.contributor.authorAzaiez, Hela
dc.contributor.authorBrownstein, Z.
dc.contributor.authorAvenarius, M. R.
dc.contributor.authorMarlin, S.
dc.contributor.authorPandya, A.
dc.contributor.authorShahin, H.
dc.contributor.authorSiemering, K. R.
dc.contributor.authorWeil, D.
dc.contributor.authorWuyts, W.
dc.contributor.authorAguirre, L.A.
dc.contributor.authorMartín, Y.
dc.contributor.authorMoreno Pelayo, Miguel Angel
dc.contributor.authorVillamar, M.
dc.contributor.authorAvraham, K. B.
dc.contributor.authorDahl, H-H M
dc.contributor.authorKanaan, M.
dc.contributor.authorNance, W. E.
dc.contributor.authorPetit, C.
dc.contributor.authorSmith, Richard J.H.
dc.contributor.authorVan Camp, Guy
dc.contributor.authorSartorato, E. L.
dc.contributor.authorMurgia, A.
dc.contributor.authorMoreno, F.
dc.contributor.authordel Castillo, I.
dc.date.accessioned2024-02-12T15:12:56Z
dc.date.available2024-02-12T15:12:56Z
dc.date.created2005
dc.date.issued2005
dc.formatapplication/pdfes_ES
dc.identifier.locationN/Aes_ES
dc.identifier.urihttps://hdl.handle.net/20.500.12080/39730
dc.languageenges_ES
dc.rightsCC-BYes_ES
dc.rights.accessrightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.eses_ES
dc.titleA novel deletion involving the connexin-30 gene, del(GJB6- d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairmentes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES

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