Search Results - Hewawitharana, G.P

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    P3.21 A missense mutation in Mitofusin 2 causing early onset, progressive, axonal polyneuropathy (CMT2), optic atrophy and developmental delay in a child

    P3.21 A missense mutation in Mitofusin 2 causing early onset, progressive, axonal polyneuropathy (CMT2), optic atrophy and developmental delay in a child by Hewawitharana, G.P, Antoniadi, T, Faulkner, C, Williams, M, Rankin, J, Majumdar, A

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