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1
CGE.13032
CGE.13032
http://dx.doi.org/10.1111/CGE.13032
A recognizable systemic connective tissue disorder with polyvalvular heart dystrophy and dysmorphism associated with TAB2 mutations.
P356
Q48307234-A16ABE87-FBF6-4C83-99A7-DF94F201DA59
P356
CGE.13032
http://dx.doi.org/10.1111/CGE.13032