Response to: Phenotypic heterogeneity of Leigh syndrome due to NDUFA12 variants is multicausal
Articolo
Data di Pubblicazione:
2022
Citazione:
Response to: Phenotypic heterogeneity of Leigh syndrome due to NDUFA12 variants is multicausal / A. Torraco, R. Maroofian, A. Rotig, E. Bertini, D. Ghezzi, R. Carrozzo, D. Diodato. - In: HUMAN MUTATION. - ISSN 1059-7794. - 43:1(2022 Jan), pp. 99-100. [10.1002/humu.24303]
Tipologia IRIS:
01 - Articolo su periodico
Keywords:
Leigh syndrome; NADH ubiquinone oxidoreductase; NDUFA12; mitochondrial disease
Elenco autori:
A. Torraco, R. Maroofian, A. Rotig, E. Bertini, D. Ghezzi, R. Carrozzo, D. Diodato
Link alla scheda completa: