← Evidence map

ArticleHuman genome variation2024

Rare mosaic variant of GJA1 in a patient with a neurodevelopmental disorder.

Rina Shimomura et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

3 papers cite it

2024
2025
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 38221519