A missense mutation in Mitofusin 2 (MFN2) causing early onset, progressive, axonal polyneuropathy (CMT2), optic atrophy and developmental delay in a child

G P Hewawitharana, T Antoniadi, C Faulkner, M Williams, J Rankin, Anirban Majumdar

Research output: Chapter in Book/Report/Conference proceedingConference Contribution (Conference Proceeding)

Original languageEnglish
Title of host publicationWorld Muscle Society 2011
Publication statusPublished - 2011

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