Marc Ferré
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0000-0001-8265-7249
46 papers found
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Reversible optic neuropathy with OPA1 exon 5b mutation
Carotid artery dissection in an adult with the Simpson–Golabi–Behmel syndrome
Mitochondrial coupling defect in Charcot-Marie-Tooth type 2A disease
Genotype-phenotype correlation in mitochondrial optic neuropathies
eOPA1: An online database forOPA1mutations
Mitochondrial diseases preferentially involve proteins with prokaryote homologues
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