You are here

  • Home
  • Archive
  • Volume 42, Issue 7
  • 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

Article Text

Article menu
Download PDFPDF
Letters to JMG
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://doi.org/10.1136/jmg.2004.028324

Statistics from Altmetric.com

    Request Permissions

    If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

    Footnotes

    • ↵* These authors contributed equally to this work

    • We thank the patients and their relatives for their kind cooperation in this study, and FIAPAS for their enthusiastic support of this research. FJdC and MV were recipients of fellowships from the Comunidad de Madrid. MRB and AA were recipients of fellowships from Fondo de Investigaciones Sanitarias. LA was a recipient of a fellowship from the Organización Nacional de Ciegos Españoles. This work was supported by grants from the European Community (QLG2-CT-1999-00988), CAICYT of Spanish Ministerio de Ciencia y Tecnología (SAF2002-03966, to FM), Spanish Research Network on the Genetic and Molecular Bases of Hearing Disorders (FIS G03/203, to FM), Programa Ramón y Cajal (to IdC), Spanish Fondo de Investigaciones Sanitarias (FIS PI020807, to IdC), the Israel Ministry of Science and Technology (to KBA), and the National Institutes of Health (RO1-DC02842, to RJHS).

    • Competing interests: none declared