← Evidence map

ArticleNeurogenetics2020

The first biallelic missense mutation in the FXN gene in a consanguineous Turkish family with Charcot-Marie-Tooth-like phenotype.

Ayşe Candayan et al.PubMed ↗Publisher ↗

No numbers read from the abstract.

13 papers cite it

2020
2021
2022
2023
2024
2025
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 31673878