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Early-onset Behr syndrome due to compound heterozygous mutations in OPA1
Download from doi.orgAre zona pellucida genes involved in recurrent oocyte lysis observed during in vitro fertilization?
Download from link.springer.comIs ABCC6 a genuine mitochondrial protein?
Download from link.springer.comPrevalence of rare mitochondrial DNA mutations in mitochondrial disorders
Download from www.ncbi.nlm.nih.govSensorineural hearing loss in OPA1-linked disorders
Download from doi.orgHereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutation
UploadLes atrophies optiques héréditaires
UploadOPA1-associated disorders: Phenotypes and pathophysiology
UploadHereditary optic neuropathies share a common mitochondrial coupling defect.
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