← Evidence map

ArticleHuman genetics2012

Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystonia.

Jose Felix Marti-Masso et al.PubMed ↗Publisher ↗

No numbers read from the abstract.

14 papers cite it

2012
2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
2025
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 21912879