Publication | Open Access
Identification of a locus (LCA9) for Leber's congenital amaurosis on chromosome 1p36
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Citations
14
References
2003
Year
Allelic VariantGenetic DisorderGeneticsPathologyLeber Hereditary Optic NeuropathyMolecular GeneticsCongenital AmaurosisDisease Gene IdentificationGenomicsMedicineMonogenic DisordersChromosome 1P36
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