A Novel Locus for Familial Amyotrophic Lateral Sclerosis, on Chromosome 18q Collette K. Hand, Jawad Khoris, François Salachas, François Gros-Louis, Ana.

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A Novel Locus for Familial Amyotrophic Lateral Sclerosis, on Chromosome 18q Collette K. Hand, Jawad Khoris, François Salachas, François Gros-Louis, Ana Amélia Simões Lopes, Veronique Mayeux-Portas, Robert H. Brown, Vincent Meininger, William Camu, Guy A. Rouleau The American Journal of Human Genetics Volume 70, Issue 1, Pages 251-256 (January 2002) DOI: 10.1086/337945 Copyright © 2002 The American Society of Human Genetics Terms and Conditions

Figure 1 Informative section of pedigree Fr017. Individuals available for typing are indicated by the generated genotype data. The markers examined are shown. Alleles in parentheses are inferred. All inferred haplotypes were reconstructed on the basis of minimal recombinations. A solid black bar indicates the disease haplotype. A thin black line denotes an unknown or unphased haplotype. Key recombinants (IV:37 and IV:67) are indicated by an asterisk (*). Alleles given refer to the Fondation Jean Dausset CEPH alleles, when available. Information is shown only for relevant individuals. To preserve confidentiality, the sex of all individuals has been disguised; in addition, six unaffected haplotype carriers have been omitted from the pedigree. The American Journal of Human Genetics 2002 70, 251-256DOI: (10.1086/337945) Copyright © 2002 The American Society of Human Genetics Terms and Conditions