Publication | Open Access
Comprehensive genotyping reveals RPE65 as the most frequently mutated gene in Leber congenital amaurosis in Denmark
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Citations
35
References
2015
Year
BiologyMendelian DisorderGenetic DisorderMedicineGeneticsGenetic MechanismMolecular GeneticsDisease Gene IdentificationGenomicsLeber Congenital AmaurosisMolecular Diagnostics
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