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Paper Details

Mutations in MYO9B are associated with Charcot-Marie-Tooth disease type 2 neuropathies and isolated optic atrophy.
Eur J Neurol
1
2023
CMT, CMT2, Charcot-Marie-Tooth disease, Charcot-Marie-Tooth disease type 2 neuropathies, MYO9B, MYO9B (myosin IX) gene, MYO9B motor domain, MYO9B mutations, Myo9b, OA, axonal neuropathies, central nervous system axons, degenerating axons, disease genes, human, isolated, isolated OA, isolated optic atrophy, mouse, myosin IX, myosin motor, optic atrophy, patients, variants
Author NameAffiliation
Dejan LazarevicCenter for Omics Sciences, IRCCS Ospedale San Raffaele
Stephan Z??chnerDepartment of Human Genetics and Hussman Institute for Human Genomics, University of Miami
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Release 1.2