Mutations of the mitochondrial carrier translocase channel subunit TIM22 cause early-onset mitochondrial myopathy.

Name: Mutations of the mitochondrial carrier translocase channel subunit TIM22 cause early-onset mitochondrial myopathy.
Author: Pacheu-Grau, David

Mutations of the mitochondrial carrier translocase channel subunit TIM22 cause early-onset mitochondrial myopathy. — المؤلف: Pacheu-Grau, David — Human molecular genetics 20190516

المؤلف: Pacheu-Grau, David
النشر: Human molecular genetics 20190516
الوصف: 4135-4144 p.
الموضوعات: Carrier Proteins؛ Child؛ DNA, Mitochondrial؛ Female؛ Fibroblasts؛ Genetic Predisposition to Disease؛ Humans؛ Lactic Acid