SUCLG1 mutations and mitochondrial encephalomyopathy: a case study and review of the literature

The mitochondrial encephalomyopathies represent a clinically heterogeneous group of neurodegenerative disorders. The clinical phenotype of patients could be explained by mutations of mitochondria-related genes, notably  SUCLG1  and  SUCLA2 . Here, we presented a 5-year-old boy with clinical features...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Molecular biology reports 2020-12, Vol.47 (12), p.9699-9714
Hauptverfasser: Molaei Ramsheh, Samira, Erfanian Omidvar, Maryam, Tabasinezhad, Maryam, Alipoor, Behnam, Salmani, Tayyeb Ali, Ghaedi, Hamid
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!