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. 2012 Dec 12;6(1):65–80. doi: 10.1007/s12265-012-9425-0

Fig. 3.

Fig. 3

Bidirectional automated sequencing of MYBPC3 exon7 and MYH7 exon35 and flanking intronic sequences in index patient PU1 and screening of an affected brother (PU1′a) showing cosegregation of MYBPC3 intron 7 substitution mutation: c.821 + 3G > T with potential splice effect as predicted by in silico tools and not MYH7 missense variant (Arg1662His) indicating likely pathogenicity of the MYBPC3 intronic variant