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Recommendations for the predictive genetic test in Huntington's disease

  1. R MacLeod1,†,‡,*,
  2. A Tibben2,†,‡,
  3. M Frontali3,†,
  4. G Evers-Kiebooms4,†,
  5. A Jones5,‡,
  6. A Martinez-Descales6,†,‡,
  7. RA Roos7,†,‡,
  8. Editorial Committee and Working Group ‘Genetic Testing Counselling’ of the European Huntington Disease Network

Article first published online: 29 JUL 2012

DOI: 10.1111/j.1399-0004.2012.01900.x

Issue

Clinical Genetics

Clinical Genetics

Volume 83, Issue 3, pages 221–231, March 2013

Additional Information

How to Cite

MacLeod R, Tibben A, Frontali M, Evers-Kiebooms G, Jones A, Martinez-Descales A, Roos RA and Editorial Committee and Working Group ‘Genetic Testing Counselling’ of the European Huntington Disease Network. Recommendations for the predictive genetic test in Huntington's disease

Author Information

  1. 1

    Genetic Medicine, Manchester Academic Health Science Centre, Central Manchester University Hospitals NHS Foundation Trust, Manchester, UK

  2. 2

    Centre for Human and Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands

  3. 3

    Istituto di Farmacologia Traslazionale del CNR, Rome, Italy

  4. 4

    Department of Human Genetics, University of Leuven, Leuven, Belgium

  5. 5

    International Huntington Association, c/o Huntington's WA (inc) The Niche, Nedlands, Western Australia, Australia

  6. 6

    Neurological Department, Fundación Jiménez Díaz Avda, Madrid, Spain

  7. 7

    Department of Neurology Leiden, University Medical Centre, Leiden, The Netherlands

  1. †

    EHDN WG Genetic Testing and Counselling: Emilia Bijlsma, Ellen Blinkenberg, Yvonne Bombard, Pascal Borry, David Craufurd, Mary Davis, Christine de Die-Smulders, Claudia Downing, Alexandra Dürr, Maria Garcia Barcina, Ruth Glew, Arvid Heiberg, Frances Heydon, Dorota Hoffman-Zacharsk, Ulrika Hösterey Ugander, Maria José Trujillo Tiebas, Wioletta Krysa, Inge Liebaers, Christiane Lohkamp, Paola Mandich, Caterina Mariotti, Bea De Schepper, Emilio di Maria, Andrea Nemeth, Oliver Quarrell, Pascale Ribaï, Alicia Semaka, Sara Seneca, Jorge Sequeiros, Ferdinando Squitieri, Anna Sulek, Lucienne van der Meer, Christine Verellen-Dumoulin, Guido de Wert.

  2. ‡

    Editorial committee: Martin Delatycki, Mark Guttman, Michael Hayden, Martha Nance, Fiona Richards, Louise Vetter.

* Corresponding author: Dr Rhona MacLeod, Genetic Medicine, Manchester Academic Health Science Centre, Central Manchester University Hospitals NHS Foundation Trust, Manchester, UK.
Tel.: +44 161 276 6510;
fax: +44 161 276 6145;
e-mail: rhona.macleod@cmft.nhs.uk

  1. †

    EHDN WG Genetic Testing and Counselling: Emilia Bijlsma, Ellen Blinkenberg, Yvonne Bombard, Pascal Borry, David Craufurd, Mary Davis, Christine de Die-Smulders, Claudia Downing, Alexandra Dürr, Maria Garcia Barcina, Ruth Glew, Arvid Heiberg, Frances Heydon, Dorota Hoffman-Zacharsk, Ulrika Hösterey Ugander, Maria José Trujillo Tiebas, Wioletta Krysa, Inge Liebaers, Christiane Lohkamp, Paola Mandich, Caterina Mariotti, Bea De Schepper, Emilio di Maria, Andrea Nemeth, Oliver Quarrell, Pascale Ribaï, Alicia Semaka, Sara Seneca, Jorge Sequeiros, Ferdinando Squitieri, Anna Sulek, Lucienne van der Meer, Christine Verellen-Dumoulin, Guido de Wert.

  2. ‡

    Editorial committee: Martin Delatycki, Mark Guttman, Michael Hayden, Martha Nance, Fiona Richards, Louise Vetter.

Publication History

  1. Issue published online: 18 FEB 2013
  2. Article first published online: 29 JUL 2012
  3. Accepted manuscript online: 29 MAY 2012 08:43AM EST
  4. Manuscript Accepted: 22 MAY 2012
  5. Manuscript Revised: 8 MAY 2012
  6. Manuscript Received: 27 MAR 2012

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