Identification of novel mitochondrial localization signals in human Tafazzin, the cause of the inherited cardiomyopathic disorder Barth syndrome
Author:
Funder
Barth Syndrome Foundation
NIH
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine,Molecular Biology
Reference35 articles.
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3. Barth syndrome: TAZ gene mutations, mRNAs, and evolution;Gonzalez;Am. J. Med. Genet. A,2005
4. Tafazzin splice variants and mutations in Barth syndrome;Kirwin;Mol. Genet. Metab.,2014
5. The enzymatic function of tafazzin;Xu;J. Biol. Chem.,2006
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2. Analysis of tafazzin and deoxyribonuclease 1 like 1 transcripts and X chromosome sequencing in the evaluation of the effect of mosaicism in the TAZ gene on phenotypes in a family affected by Barth syndrome;Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis;2023-01
3. Current and future treatment approaches for Barth syndrome;Journal of Inherited Metabolic Disease;2021-11-10
4. Metabolic Alterations Caused by Defective Cardiolipin Remodeling in Inherited Cardiomyopathies;Life;2020-11-11
5. Barth syndrome cardiomyopathy: targeting the mitochondria with elamipretide;Heart Failure Reviews;2020-10-01
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