Fig. 5From: Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis ImperfectaAll the published WNT1 mutations associated with recessive OI. Red arrow with red text shows all the stop mutations. Red arrow with blue text point mutations. Blue wedge represents the duplication or deletions. Yellow wedge shows our novel mutation (Figure is made up to scale)Back to article page