← Evidence map

ArticleOrphanet journal of rare diseases2022

Identification of three novel homozygous variants in COL9A3 causing autosomal recessive Stickler syndrome.

Aboulfazl Rad et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

7 papers cite it

2022
2023
2024
2025
2026
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 35241111