A common ancestor for COCH related cochleovestibular (DFNA9) patients in Belgium and The Netherlands bearing the P51S mutation

Fransen, E;Verstreken, M;Bom, SJH;Lemaire, F;Van Camp, G.;et.al.
(2001) Journal of Medical Genetics : an international peer-reviewed journal for health professionals and researchers in all areas of genetics — Vol. 38, n° 1, p. 61-64 (2001)

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  • Fransen, E
    Author
  • Verstreken, M
    Author
  • Bom, SJH
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  • Lemaire, F
    Author
  • Van Camp, G.
    Author
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Fransen, E., Verstreken, M., Bom, S., Lemaire, F., Kemperman, M., De Kok, Y., Wuyts, F., Verhagen, W., Huygen, P., McGuirt, W., Smith, R., Van Maldergem, L., Declau, F., Cremers, C., Van de Heyning, P., Cremers, F., & Van Camp, G. (2001). A common ancestor for COCH related cochleovestibular (DFNA9) patients in Belgium and The Netherlands bearing the P51S mutation. Journal of Medical Genetics : an international peer-reviewed journal for health professionals and researchers in all areas of genetics, 38(1), 61-64. https://doi.org/10.1136/jmg.38.1.61 (Original work published 2001)