← Evidence map

ArticleHGG advances2026

Biallelic variants in CHCHD4 are associated with combined OXPHOS defect leading to mitochondrial disease.

Matthieu Mantecon et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

Not cited yet

Full record →Abstract, authors, funding and every citing paper · PMID 41981912