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. Author manuscript; available in PMC: 2011 Sep 15.
Published in final edited form as: J Neurol Sci. 2010 Jul 14;296(1-2):22–29. doi: 10.1016/j.jns.2010.06.017

Figure 2.

Figure 2

Sequence chromatograms for a portion of exon 5 of FHL1 showing a mutation in the family with X-linked scapuloperoneal myopathy compared to a control with the wild-type nucleotide c at nt 366 (A). A hemizygous g to c transversion in an affected subject (B) and heterozygous g to c change in his mother (C) that predicts substitution of tryptophan for cysteine in residue 122 (W122C). W122C co-segregated with disease in the family and was not present in 338 normal control X-chromosomes.