Evidence of autosomal dominant Leber congenital amaurosis (LCA) underlain by a CRX heterozygous null allele
- PMID: 12843339
- PMCID: PMC1735514
- DOI: 10.1136/jmg.40.7.e90
Evidence of autosomal dominant Leber congenital amaurosis (LCA) underlain by a CRX heterozygous null allele
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