Cite
HARVARD Citation
Cipriani, S. et al. (2023). Mutations in MYO9B are associated with Charcot–Marie–Tooth disease type 2 neuropathies and isolated optic atrophy. European journal of neurology. pp. 511-526. [Online].
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Cipriani, S. et al. (2023). Mutations in MYO9B are associated with Charcot–Marie–Tooth disease type 2 neuropathies and isolated optic atrophy. European journal of neurology. pp. 511-526. [Online].