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Autor:
Frida Mandik, Yuliia Kanana, Jost Rody, Sophie Misera, Bernd Wilken, Björn-Hergen Laabs von Holt, Christine Klein, Melissa Vos
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 10 (2022)
Fatty acid hydroxylase-associated neurodegeneration (FAHN) is a rare disease that exhibits brain modifications and motor dysfunctions in early childhood. The condition is caused by a homozygous or compound heterozygous mutation in fatty acid 2 hydrox
Externí odkaz:
https://doaj.org/article/cbfa4ab939774d59ab40eef54e1c88bb
