Infantile mitochondrial encephalomyopathy with unusual phenotype caused by a novel BCS1L mutation in an isolated complex III-deficient patient
Alberto Blázquez, Mari Carmen Gil-Borlado, María Morán, Alfonso Verdú, María Rosario Cazorla-Calleja, Miguel A. Martín, Joaquín Arenas, Cristina UgaldeVolume:
19
Year:
2009
Language:
english
DOI:
10.1016/j.nmd.2008.11.016
File:
PDF, 225 KB
english, 2009