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- W2023229609 abstract "Barth syndrome (BTHS) is a rare X-linked disorder characterized by cardiomyopathy, short stature, neutropenia, and 3-methylglutaconic aciduria. Mutations have been identified in the TAZ (G4.5) gene in patients with BTHS. This article presents a mutation analysis of this gene in a Japanese boy with cardiomyopathy with abnormal mitochondria, cyclic neutropenia, and 3-methylglutaconic aciduria (type 2). The analysis revealed a novel missense mutation (R94S) caused by a single nucleotide substitution (C-to-A) in this patient." @default.
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- W2023229609 date "2002-05-01" @default.
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- W2023229609 title "Novel missense mutation (R94S) in the TAZ (G4.5) gene in a Japanese patient with Barth syndrome" @default.
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- W2023229609 doi "https://doi.org/10.1007/s100380200030" @default.
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