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A Novel Missense Mutation of GATA4 in a Chinese Family with Congenital Heart Disease.

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Academic year: 2017

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Fig 1. GATA4 mutation segregates with familial CHD. Family members in the pedigree chart are indicated by generations (I-III) and numbers
Fig 2. Distribution of the identified GATA4 mutation and multiple sequence alignment of GATA4 protein
Fig 3. Disease-causing potential of the GATA4 mutation. (A) Functional significance of mutation prediction done by SIFT, PolyPhen-2 and MutationTaster
Fig 5. Expression levels of GATA4 wide-type and p.R311W mutant protein in Hela cells. Western blot exhibits equal amount of GATA4 p.R311W protein as compared to the wild-type

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