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Barth Syndrome — Gene Therapy & Clinical Trials | FollowGene

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Barth Syndrome

Prevalence: 1/300000

cardiac

Official·OMIM:302060 Official·ORPHA111

Cardiomyopathy, neutropenia, and myopathy due to TAZ gene mutations.

Associated Genes

TAFAZZINTafazzin

Chromosome XX-Linked Recessive

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