Guy Lenaers
CNRS Délégation Bretagne et Pays de Loire
17 papers found
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TEFM variants impair mitochondrial transcription causing childhood-onset neurological disease
Download from doi.orgPhysiology of PNS axons relies on glycolytic metabolism in myelinating Schwann cells
Download from doi.orgACO2 clinicobiological dataset with extensive phenotype ontology annotation
Download from doi.orgDominant optic atrophy: Culprit mitochondria in the optic nerve
UploadMutations in the m-AAA proteases AFG3L2 and SPG7 are causing isolated dominant optic atrophy
Download from doi.orgA Data Mining Metabolomics Exploration of Glaucoma
Download from doi.orgDominant mutations in mtDNA maintenance gene SSBP1 cause optic atrophy and foveopathy
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