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Article

X-linked fetal cardiomyopathy caused by a novel mutation in theTAZ gene

1 Jan 2006

Abstract excerpt

OBJECTIVES: Mutations in the tafazzin (TAZ) gene at chromosomal locus Xq28 are responsible for Barth syndrome (BTHS), X-linked endocardial fibroelastosis (EFE), X-linked fatal infantile dilated cardiomyopathy (CMD3A), and familial isolated noncompaction of left ventricular myocardium (INVM). This evaluation was performed to determine if a known familial TAZ gene mutation might present with abnormal fetal cardiac...

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Identifiers

PMID: 16548007
DOI: 10.1002/pd.1438

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