← Evidence map

ArticleGenetics in medicine : official journal of the American College of Medical Genetics2021

Heterozygous truncating variants in SUFU cause congenital ocular motor apraxia.

Simone Schröder et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

10 papers cite it

2021
2022
2023
2024
2025
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 33024317