← Evidence map

ArticleHuman mutation2013

Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12.

Guida Landouré et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

50 papers cite it

2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
2025
2026
this paperpooled itcites it
Full record →Abstract, authors, funding and every citing paper · PMID 23857908