Search Results - "Harris, Kodi Williams" :: K.UTB vyhledávací portál

Use of novel iPSC-derived skeletal muscle model to understand mitochondrial phenotypes of TAFAZZIN-deficiency in Barth syndrome

by Lee, Kyuna, Carney, Olivia Sniezek, Harris, Kodi Williams, Vernon, Hilary
Published in Molecular genetics and metabolism (01.04.2024)

Get full text

Journal Article

Loading…

Defective cardiomyocyte mitophagy in TAFAZZIN deficiency: New implications for cellular pathogenesis in Barth syndrome

by Carney, Olivia Sniezek, Lee, Kyuna, Harris, Kodi Williams, Butschek, Grant, Anzmann, Arianna, Hammacher-Brady, Anne, Vernon, Hilary
Published in Molecular genetics and metabolism (01.04.2024)

Get full text

Journal Article

Use of novel iPSC-derived skeletal muscle model to understand mitochondrial phenotypes of TAFAZZIN-deficiency in Barth syndrome

Defective cardiomyocyte mitophagy in TAFAZZIN deficiency: New implications for cellular pathogenesis in Barth syndrome

Refine Results

Format

Subject Area

Language

Year of Publication

Database