Erratum: Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family

European Journal of Human Genetics volume 8, page468(2000)Cite this article

The Original Article was published on 01 February 2000

Download PDF
Authors
  1. David P Kelsell
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Amanda L Wilgoss
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Gabriela Richard
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Howard P Stevens
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Colin S Munro
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Irene M Leigh
    View author publications

    You can also search for this author in PubMed Google Scholar

Additional information

The online version of the original article can be found at 10.1038/sj.ejhg.5200407

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Kelsell, D., Wilgoss, A., Richard, G. et al. Erratum: Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family. Eur J Hum Genet 8, 468 (2000). https://doi.org/10.1038/sj.ejhg.5200510

Download citation

Further reading

Search

Quick links