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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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APA

del Castillo, F. J. & Rodríguez Ballesteros, M. & Álvarez, A. & Hutchin, T. & Leonardi, E. & de Oliveira, C. A. & Azaiez, Hela & Brownstein, Z. & Avenarius, M. R. & Marlin, S. & Pandya, A. & Shahin, H. & Siemering, K. R. & Weil, D. & Wuyts, W. & Aguirre, L.A. & Martín, Y. & Moreno Pelayo, Miguel Angel & Villamar, M. & Avraham, K. B. & Dahl, H-H M & Kanaan, M. & Nance, W. E. & Petit, C. & Smith, Richard J.H. & Van Camp, Guy & Sartorato, E. L. & Murgia, A. & Moreno, F. & del Castillo, I. (2005 ) .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.

ISO 690

del Castillo, F. J. & Rodríguez Ballesteros, M. & Álvarez, A. & Hutchin, T. & Leonardi, E. & de Oliveira, C. A. & Azaiez, Hela & Brownstein, Z. & Avenarius, M. R. & Marlin, S. & Pandya, A. & Shahin, H. & Siemering, K. R. & Weil, D. & Wuyts, W. & Aguirre, L.A. & Martín, Y. & Moreno Pelayo, Miguel Angel & Villamar, M. & Avraham, K. B. & Dahl, H-H M & Kanaan, M. & Nance, W. E. & Petit, C. & Smith, Richard J.H. & Van Camp, Guy & Sartorato, E. L. & Murgia, A. & Moreno, F. & del Castillo, I.. 2005 .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.

https://hdl.handle.net/20.500.12080/39730
dc.contributor.author del Castillo, F. J.
dc.contributor.author Rodríguez Ballesteros, M.
dc.contributor.author Álvarez, A.
dc.contributor.author Hutchin, T.
dc.contributor.author Leonardi, E.
dc.contributor.author de Oliveira, C. A.
dc.contributor.author Azaiez, Hela
dc.contributor.author Brownstein, Z.
dc.contributor.author Avenarius, M. R.
dc.contributor.author Marlin, S.
dc.contributor.author Pandya, A.
dc.contributor.author Shahin, H.
dc.contributor.author Siemering, K. R.
dc.contributor.author Weil, D.
dc.contributor.author Wuyts, W.
dc.contributor.author Aguirre, L.A.
dc.contributor.author Martín, Y.
dc.contributor.author Moreno Pelayo, Miguel Angel
dc.contributor.author Villamar, M.
dc.contributor.author Avraham, K. B.
dc.contributor.author Dahl, H-H M
dc.contributor.author Kanaan, M.
dc.contributor.author Nance, W. E.
dc.contributor.author Petit, C.
dc.contributor.author Smith, Richard J.H.
dc.contributor.author Van Camp, Guy
dc.contributor.author Sartorato, E. L.
dc.contributor.author Murgia, A.
dc.contributor.author Moreno, F.
dc.contributor.author del Castillo, I.
dc.date.accessioned 2024-02-12T15:12:56Z
dc.date.available 2024-02-12T15:12:56Z
dc.date.created 2005
dc.date.issued 2005
dc.identifier.uri https://hdl.handle.net/20.500.12080/39730
dc.format application/pdf es_ES
dc.language eng es_ES
dc.rights CC-BY es_ES
dc.rights.uri http://creativecommons.org/licenses/by/4.0/deed.es es_ES
dc.title 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 es_ES
dc.type info:eu-repo/semantics/article es_ES
dc.rights.accessrights info:eu-repo/semantics/openAccess es_ES
dc.identifier.location N/A es_ES


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