Publication | Closed Access
OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28
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Citations
23
References
2000
Year
Mendelian DisorderDynamin-related GtpaseGenetic DisorderGeneticsMolecular GeneticsDisease Gene IdentificationSystems BiologyMedicineVariant Interpretation
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