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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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del Castillo, F J & Rodríguez Ballesteros, M & Álvarez, A & Hutchin, T & Leonardi, E & de Oliveira, C A & Azaiez, H & 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, R J H & Van Camp, G & 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, H & 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, R J H & Van Camp, G & 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, H
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, R J H
dc.contributor.author Van Camp, G
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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