← Evidence map

ArticleBrain : a journal of neurology2017

A recurrent de novo mutation in TMEM106B causes hypomyelinating leukodystrophy.

Cas Simons et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

54 papers cite it

2017
2018
2019
2020
2021
2022
2023
2024
2025
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 29186371