Autosomal-dominant Leber Congenital Amaurosis Caused by a Heterozygous CRX Mutation in a Father and Son

Reference

Arcot Sadagopan, Karthikeyan, et al. “Autosomal-Dominant Leber Congenital Amaurosis Caused by a Heterozygous CRX Mutation in a Father and Son”. Ophthalmic Genetics, vol. 36, no. 2, Sept. 2013, pp. 156–159, https://doi.org/10.3109/13816810.2013.838273.

PubMed Reference Number (PMID)

24093488