MRPS34

Combined oxidative phosphorylation deficiency type 32 (COXPD32) / Leigh spectrum

1 article(s) in the watch · Constitutional genetics

Curated publications

Expanding the clinical and genetic spectrum of MRPS34-related disease: two new cases and systematic review.

Combined oxidative phosphorylation deficiency type 32 (COXPD32) / Leigh spectrum

Automatic aggregation page — a clinical introduction may be added.