← Evidence map

ArticleEuropean journal of human genetics : EJHG2026

A systematic analysis of mitochondrial aminoacyl tRNA synthetase variants in a rare disease cohort.

Thiloka E Ratnaike 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 41454053