P3.21 A missense mutation in Mitofusin 2 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, A. MajumdarVolume:
21
Year:
2011
Language:
english
DOI:
10.1016/j.nmd.2011.06.915
File:
PDF, 47 KB
english, 2011