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Fig. 1 | BMC Neurology

Fig. 1

From: Clinical characteristics and proteome modifications in two Charcot-Marie-Tooth families with the AARS1 Arg326Trp mutation

Fig. 1

Pedigree and haplotype analysis. A Two CMT2 pedigrees and segregation of the AARS1 and ATL1 variants. Arrows = proband; black colour fillings = affected by CMT/CMT2; black lines filling = affected by HSP; black dot = obligate AARS1 carrier, not clinically examined; wt = wild type. B Haplotype analysis results for six individuals from two families; Family 1: II-2 II-3 and II-7, Family 2: II-1, II.2 and III-2 depicted for chromosome 16. The AARS1 gene and markers shared between the two families are marked to the figure. The ideogram of chromosome 16 was downloaded from https://www.ncbi.nlm.nih.gov/genome/tools/gdp according to the GRCh37/hg19 assembly

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BMC Neurology

ISSN: 1471-2377

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