← Evidence map

ArticleJournal of human genetics2020

What is the ocular phenotype associated with a single exon 78 deletion in Duchenne muscular dystrophy?

Tuy Nga Brignol et al.PubMed ↗Publisher ↗

No numbers read from the abstract.

Not cited yet

Full record →Abstract, authors, funding and every citing paper · PMID 32451493