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S0002-9394(01)01187-4
S0002-9394(01)01187-4
http://dx.doi.org/10.1016/S0002-9394(01)01187-4
Isolated late-onset cone-rod dystrophy revealing a familial neurogenic muscle weakness, ataxia, and retinitis pigmentosa syndrome with the T8993G mitochondrial mutation.
P356
Q39364834-1C225D86-3CAA-4D49-BB11-FA335E73AFBF
P356
S0002-9394(01)01187-4
http://dx.doi.org/10.1016/S0002-9394(01)01187-4