Mitochondrial encephalomyopathy with coenzyme Q <sub>10</sub> deficiency
Cláudia Ferreira da Rosa Sobreira(Universidade de São Paulo), S. DiMauro(Columbia University), Amilton Antunes Barreira(National Cancer Center), Edgar Davidson(Integral Molecular (United States)), Ronald G. Haller(The University of Texas Southwestern Medical Center), Filippo M. Santorelli(Fondazione Stella Maris), Sara Shanske(Columbia University), Ramsi Keller(NewYork–Presbyterian Hospital), Michio Hirano(Columbia University Irving Medical Center), Armand F. Miranda(Columbia University), Daniel S. Mojon(Hospital Del Mar), E. Bonilla(NewYork–Presbyterian Hospital), Michael P. King(Thomas Jefferson University)
Cited by 196
Related Papers
Mitochondrial diseases
|Nature Reviews Disease Primers|2016|1.5k
Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)
|Nature|2000|941
Human mitochondrial DNA: roles of inherited and somatic mutations
|Nature Reviews Genetics|2012|747
Diagnosis and management of mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society
|Genetics in Medicine|2014|605