4.5 Article

The chromosome 9 ALS and FTD locus is probably derived from a single founder

Journal

NEUROBIOLOGY OF AGING
Volume 33, Issue 1, Pages -

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.neurobiolaging.2011.08.005

Keywords

Genetics; Amyotrophic lateral sclerosis; Frontotemporal dementia; Finland

Funding

  1. National Institute on Aging [Z01-AG000949-02]
  2. NIH [R01AG031278, R01AG038791]
  3. National Institute on Neurological Disorders and Stroke
  4. NIH/NIA [R01 AG26251]
  5. European Community [259867]
  6. Motor Neurone Disease Association of Great Britain
  7. ALS Association
  8. Angel Fund
  9. ALS Therapy Alliance
  10. Wellcome Trust
  11. Reta Lila Weston Foundation
  12. MRC
  13. Microsoft Research Foundation
  14. Helsinki University Central Hospital
  15. Finnish Academy
  16. Ministero della Salute
  17. Progetti Finalizzati
  18. Fondazione Vialli e Mauro for ALS
  19. Federazione Italiana Giuoco Calcio
  20. Hersenstichting Nederland
  21. NIHR specialist Biomedical Research Centre for Mental Health at the South London and Maudsley NHS Foundation Trust (SLaM)
  22. Institute of Psychiatry, King's College London
  23. NIHR
  24. NATIONAL INSTITUTE ON AGING [R01AG026251, R01AG038791, ZIAAG000934, ZIAAG000933, R01AG031278, Z01AG000949] Funding Source: NIH RePORTER
  25. MRC [MC_G1000735, G0700943, G0701441, G0701075] Funding Source: UKRI
  26. Alzheimers Research UK [ART-PG2010-1, ART-PPG2011A-14] Funding Source: researchfish
  27. Medical Research Council [G0701441, G0701075, G0801418B, MC_G1000735, G0700943] Funding Source: researchfish

Ask authors/readers for more resources

We and others have recently reported an association between amyotrophic lateral sclerosis (ALS) and single nucleotide polymorphisms on chromosome 9p21 in several populations. Here we show that the associated haplotype is the same in all populations and that several families previously shown to have genetic linkage to this region also share this haplotype. The most parsimonious explanation of these data are that there is a single founder for this form of disease. (C) 2012 Elsevier Inc. All rights reserved.

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