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Gene|October 1, 1992
Differential expression of genes specifying two isoforms of subunit VIa of human cytochrome c oxidaseG M Fabrizi, J Sadlock, M Hirano, et al.Neurology|June 1, 1985
Fatal infantile cytochrome c oxidase deficiency: decrease of immunologically detectable enzyme in muscleN Bresolin, M Zeviani, E Bonilla, et al.European Journal of Human Genetics : EJHG|January 1, 1995
Evidence of linkage between susceptibility to multiple sclerosis and HLA-class II loci in Italian multiplex familiesM Eoli, M Pandolfo, A Amoroso, et al.Muscle & Nerve|July 1, 1991
Carnitine in muscle, serum, and urine of nonprofessional athletes: effects of physical exercise, training, and L-carnitine administrationJ Arenas, J R Ricoy, A R Encinas, et al.Genomics|November 1, 1994
Order of six loci at 2q24-q31 and orientation of the HOXD locusE Rossi, A Faiella, M Zeviani, et al.Journal of the Neurological Sciences|October 16, 2007
Clinical features and new molecular findings in Carnitine Palmitoyltransferase II (CPT II) deficiencyS Corti, A Bordoni, D Ronchi, et al.Nature Genetics|February 1, 1995
An autosomal locus predisposing to deletions of mitochondrial DNAA Suomalainen, J Kaukonen, P Amati, et al.DNA and Cell Biology|November 5, 1997
Characterization and expression of the mouse endonuclease G geneE Prats, M Noël, J Létourneau, et al.Human Molecular Genetics|November 7, 2000
A novel frameshift mutation of the mtDNA COIII gene leads to impaired assembly of cytochrome c oxidase in a patient affected by Leigh-like syndromeV Tiranti, P Corona, M Greco, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 5, 2008
An apparently sporadic case of oculopharyngeal muscular dystrophy: the first Italian reportL Tremolizzo, A Galbussera, E Tagliabue, et al.Pageof 18