Lopergolo, D.; Berti, G.; Gallus, G.N.; Bianchi, S.; Santorelli, F.M.; Malandrini, A.; De Stefano, N.
The First Heterozygous TWNK Nonsense Mutation Associated with Progressive External Ophthalmoplegia: Evidence for a New Piece in the Puzzle of Mitochondrial Diseases. Biomolecules 2025, 15, 1337.
https://doi.org/10.3390/biom15091337
AMA Style
Lopergolo D, Berti G, Gallus GN, Bianchi S, Santorelli FM, Malandrini A, De Stefano N.
The First Heterozygous TWNK Nonsense Mutation Associated with Progressive External Ophthalmoplegia: Evidence for a New Piece in the Puzzle of Mitochondrial Diseases. Biomolecules. 2025; 15(9):1337.
https://doi.org/10.3390/biom15091337
Chicago/Turabian Style
Lopergolo, Diego, Gianna Berti, Gian Nicola Gallus, Silvia Bianchi, Filippo Maria Santorelli, Alessandro Malandrini, and Nicola De Stefano.
2025. "The First Heterozygous TWNK Nonsense Mutation Associated with Progressive External Ophthalmoplegia: Evidence for a New Piece in the Puzzle of Mitochondrial Diseases" Biomolecules 15, no. 9: 1337.
https://doi.org/10.3390/biom15091337
APA Style
Lopergolo, D., Berti, G., Gallus, G. N., Bianchi, S., Santorelli, F. M., Malandrini, A., & De Stefano, N.
(2025). The First Heterozygous TWNK Nonsense Mutation Associated with Progressive External Ophthalmoplegia: Evidence for a New Piece in the Puzzle of Mitochondrial Diseases. Biomolecules, 15(9), 1337.
https://doi.org/10.3390/biom15091337