Varaico: Literature-Extracted Genetic Variants

Gene:TAFAZZIN
Variant:p.I209N
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TAFAZZIN

NM_000116.5:p.I209N

Associated Papers

Identification of novel mitochondrial localization signals in human Tafazzin, the cause of the inherited cardiomyopathic disorder Barth syndrome.

Dinca AA et al.

Journal of Molecular and Cellular Cardiology, 2018

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."