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Arch Neurol. 2007 Feb;64(2):240-5.

Three families with amyotrophic lateral sclerosis and frontotemporal dementia with evidence of linkage to chromosome 9p.

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Center for the Study of Brain Diseases, University of Montreal, Centre Hospitalier de l'Université de Montréal Research Center, Notre-Dame Hospital, 1560 Sherbrooke Street E., Montreal, Quebec, Canada.

Erratum in

  • Arch Neurol. 2007 Jun;64(6):909. Salachas, François [added].



Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are neurodegenerative disorders with adult onset that generally progress rapidly after the onset of symptoms. The 2 conditions are independent, but they also overlap in a significant proportion of families, including 2 families in which the disorders are reported to be linked to chromosome 9p. A locus was established between the markers D9S2154 and D9S1791 by comparing haplotypes between these families.


To determine whether additional families have ALS and FTD linked to chromosome 9p.


Families were identified in Canada and France, and genotyping was performed using sequence tagged site markers around the ALS-FTD candidate interval.


Three new families with mapping to the chromosome 9p ALS-FTD locus were identified. Analysis of the largest family shows a peak 2-point logarithm of odds (LOD) score of 2.81 and a multipoint LOD score of 3.01. The particular candidate interval delineated by this family spans 27.1 centimorgans (cM) between markers D9S157 and D9S1805. This reduces the centromeric boundary of the candidate interval compared with previously reported values, shortening the locus to 8.1 cM (8.0 megabase pairs). A maximum multipoint LOD score of 7.22 is obtained when the 3 families are combined.


The identification of new families enables reduction of the ALS-FTD candidate region located on chromosome 9p. The clinical features observed in these families help characterize the profiles of ALS and FTD with linkage to chromosome 9p-linked families.

[Indexed for MEDLINE]

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