Mutations in <i>MYO9B</i> are associated with Charcot–Marie–Tooth disease type 2 neuropathies and isolated optic atrophy - Concepedia

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Publication | Open Access

Mutations in <i>MYO9B</i> are associated with Charcot–Marie–Tooth disease type 2 neuropathies and isolated optic atrophy

DOI Full Paper Access

11

Citations

21

References

2022

Year

Silvia Cipriani, Marta Guerrero‐Valero, Stefano Tozza, Edward Zhao, Veith Vollmer, Danique Beijer, Matt C. Danzi, Cristina Rivellini, Dejan Lazarević, Giovanni Battista Pipitone,

European Journal of Neurology

Abstract

Novel or very rare variants in MYO9B are associated with CMT2 and isolated OA.

References

	Year	Citations

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