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

Mok, Kin; Traynor, Bryan J; Schymick, Jennifer; Tienari, Pentti J; Laaksovirta, Hannu; Peuralinna, Terhi; Myllykangas, Liisa; Chiò, Adriano; Shatunov, Aleksey; Boeve, Bradley F; Boxer, Adam L; Dejesus-Hernandez, Mariely; Mackenzie, Ian R; Waite, Adrian; Williams, Nigel; Morris, Huw R; Simón-Sánchez, Javier; van Swieten, John C; Heutink, Peter; Restagno, Gabriella; Mora, Gabriele; Morrison, Karen E; Shaw, Pamela J; Rollinson, Pamela Sara; Al-Chalabi, Ammar; Rademakers, Rosa; Pickering-Brown, Stuart; Orrell, Richard W; Nalls, Michael A; Hardy, John

Neurobiology of aging. 2011;.

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Abstract

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.

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Manchester eScholar ID:
uk-ac-man-scw:136608
Created by:
Caine, Morag
Created:
15th November, 2011, 14:50:10
Last modified by:
Caine, Morag
Last modified:
15th November, 2011, 14:50:10

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