← Evidence map

ArticleBMC medical genetics2020

Novel compound heterozygous TMEM67 variants in a Vietnamese family with Joubert syndrome: a case report.

Thi Phuong Hoa Bui et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

5 papers cite it

2020
2021
2022
2023
2024
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 32000717