Skip to main content

Advertisement

Fig. 2 | BMC Medical Genetics

Fig. 2

From: A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy

Fig. 2

Family pedigree showing the four affected siblings (filled symbols). Haplotypes spanning 8q24.12ā€“q24.21 are shown under each symbol with two black arrows indicating the shared homozygous region between the affected individuals. The presence of the mutant allele (c.727Gā€‰>ā€‰C) is indicated by (+). The index case is indicated by the red arrow. The number below the symbol represents the age (in years). Echocardiogram was performed on the parents of the index case and all of their offspring

Back to article page