Effects of a mutation in the HSPE1 gene encoding the mitochondrial co-chaperonin HSP10 and its potential association with a neurological and developmental disorder

by Anne Sigaard Bie, Paula Fernandez-Guerra, Rune Isak Dupont Birkler, Shahar Nisemblat, Dita Pelnena, Xinping Lu, Joshua L. Deignan, Hane Lee, Naghmeh Dorrani, Naghmeh Dorrani, Thomas Juhl Corydon, Johan Palmfeldt, Liga Bivina, Abdussalam Azem, Kristin Herman, Bross Peter
Published 2016-10-01