Expanding the phenotype of DNAJC3 mutations: A case with hypothyroidism additionally to diabetes mellitus and multisystemic neurodegeneration Response

Author(s):
Smit, R.A.J.; Cessie, S. le; Jukema, J.W. (0000-0002-3246-8359); Trompet, S.
Published
2017
Publication type
Article / Letter to editor
Date issued
2017-11-30
Language
English
Is part of
Clinical Genetics (2017), Vol. 92, no. 5, p. 565-565
hdl
1887/95087
doi
10.1111/cge.13041