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Your search keyword '"Verny, Christophe"' showing total 9 results

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9 results on '"Verny, Christophe"'

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1. Increased mitochondrial fusion in a autosomal recessive CMT2A family with mitochondrial GTPase mitofusin 2 mutations.

2. The metabolomic signature of Leber's hereditary optic neuropathy reveals endoplasmic reticulum stress.

3. New practical definitions for the diagnosis of autosomal recessive spastic ataxia of Charlevoix-Saguenay.

4. Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutation

5. Sensorineural hearing loss in OPA1-linked disorders.

6. OPA1-related disorders: Diversity of clinical expression, modes of inheritance and pathophysiology.

7. Assembly defects induce oxidative stress in inherited mitochondrial complex I deficiency.

8. Mitochondrial dysfunction and pathophysiology of Charcot–Marie–Tooth disease involving GDAP1 mutations

9. OPA1-associated disorders: Phenotypes and pathophysiology

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