Pontocerebellar hypoplasia with spinal muscular atrophy (PCH1): identification of SLC25A46 mutations in the original Dutch PCH1 family

Author(s):
Dijk, T. van; Rudnik-Schoneborn, S.; Senderek, J.; Hajmousa, G.; Mei, H.L.; Dusl, M.; Aronica, E.; Barth, P.; Baas, F.
Published
2017
Publication type
Article / Letter to editor
Date issued
2017-08-31
Language
English
Is part of
Brain (2017), Vol. 140, p. E45-+
hdl
1887/114887
doi
10.1093/brain/awx147