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Loss of function variants in myocardin cause congenital megabladder in humans and mice

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Figure

Figure 1. Identification of MYOCD variants in 4 families with congenital megabladder. (A) Pedigrees of 4 families presenting with congenital megablad-der
Figure 2. Bladder and kidney abnormalities in family A. (A and C) From healthy midgestation fetuses
Figure 4. Myocdwere quantified by qPCR using E15 bladders of WT, bladder. Bl, bladder; In, intestine; Re, rectum; U, urethelium; S, submucosa; DM, detrusor muscle

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