Distal myopathy with cachexia: an unrecognised phenotype caused by dominantly-inherited mitochondrial polymerase mutations
Pitceathly, R. D. S., Tomlinson, S. E., Hargreaves, I., Bhardwaj, N., Holton, J. L., Morrow, J. M., Evans, J., Smith, C., Fratter, C., Woodward, C. E., Sweeney, M. G., Rahman, S., Hanna, M. G.Volume:
84
Language:
english
Journal:
Journal of Neurology, Neurosurgery & Psychiatry
DOI:
10.1136/jnnp-2012-303232
Date:
January, 2013
File:
PDF, 2.17 MB
english, 2013