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Use of novel iPSC-derived skeletal muscle model to understand mitochondrial phenotypes of TAFAZZIN-deficiency in Barth syndrome.
- Source :
-
Molecular Genetics & Metabolism . Apr2024, Vol. 141 Issue 4, pN.PAG-N.PAG. 1p. - Publication Year :
- 2024
- Subjects :
- *MITOCHONDRIA
*SYNDROMES
*SKELETAL muscle
Subjects
Details
- Language :
- English
- ISSN :
- 10967192
- Volume :
- 141
- Issue :
- 4
- Database :
- Academic Search Index
- Journal :
- Molecular Genetics & Metabolism
- Publication Type :
- Academic Journal
- Accession number :
- 176440665
- Full Text :
- https://doi.org/10.1016/j.ymgme.2024.108192