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Updated: Jun 5, 2026

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The m.14484T>C MT-ND6 Mutation Presenting with a Hereditary Spastic-Paraparesis Phenotype

Gabriel Amorelli1,2,3, Christelle Nilles4, Gerald Pfeffer5,6

  • 1Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.

Movement Disorders Clinical Practice
|June 3, 2026
PubMed
Abstract

No abstract available in PubMed .

Keywords:
LHON plusataxiadegenerativehereditary spastic paraparesismitochondrial

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