Biallelic mutations in Oxa1l cause a mitochondrial encephalopathy and combined oxidative phosphorylation dysfunction
Titel:
Biallelic mutations in Oxa1l cause a mitochondrial encephalopathy and combined oxidative phosphorylation dysfunction
Auteur:
Thompson, K. Mai, N. Olahova, M. Scialo, F. Formosa, L.E. Stroud, D.A. Garett, M. Lax, N.Z. Jou, C. Nascimento, A. Ortez, C. Jimenez-Mallabrera, C. Hardy, S.A. He, L. Brown, G.K. Marttinen, P. McFarland, R. Sanz, A. Battersby, B.J. Bonnen, P.E. Ryan, M.T. Chrzanowska-Lightowlers, Z.M.A. Lightowlers, R.N. Taylor, R.W.