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. 2002 Jan 17;70(3):726–736. doi: 10.1086/339274

Figure 2.

Figure 2

Pedigree of largest Algerian family with AR-CMT2, mutant haplotypes, and integrated map at the LMNA locus. A, Pedigrees and genotypes of Algerian families ALG.16-301 and ALG.16-315, both with AR-CMT2. Blackened symbols represent subjects with clinical, electrophysiological, and histological diagnosis of CMT2. The homozygosity interval in each affected individual is boxed and shaded. B, Genetic, physical, and partial transcriptional map of 1q21.2-q21.3 region. The common haplotype for D1S303, D1S2777, and D1S2721 that is shared by all affected individuals from the three Algerian families is shown (see “Results” section). Position of genetic markers is indicated with two-point LOD-score values. The positions of A1U, SEMB, and LMNA are indicated.