Iris M. Wijnen
Nijmegen, GE, Netherlands
Last Updated: 09/26/2026
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Found 2 publications
De novo variants in CAMTA1 cause a syndrome variably associated with spasticity, ataxia, and intellectual disability.
Journal: European journal of human genetics : EJHG
Published: April 09, 2019
A zebrafish model to study small-fiber neuropathy reveals a potential role for GDAP1.
Journal: Mitochondrion
Published: March 23, 2018
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Last Updated: 09/26/2026