← Evidence map

ArticleAnnals of neurology2018

Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects.

Eunju Seong et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

115 papers cite itlatest 60 shown

2018
…
2022
2023
2024
2025
2026
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 29604224