Sporadic myopathy, myoclonus, leukoencephalopathy, neurosensory deafness, hypertrophic cardiomyopathy and insulin resistance associated with the mitochondrial 8306 T>C MTTK mutation
Elena Cardaioli, Edoardo Malfatti, Carla Battisti, Paola Da Pozzo, Anna Rubegni, Gian Nicola Gallus, Alessandro Malandrini, Antonio FedericoVolume:
321
Year:
2012
Language:
english
DOI:
10.1016/j.jns.2012.07.027
File:
PDF, 559 KB
english, 2012