Recessive Mutations in KCNJ13, Encoding an Inwardly Rectifying Potassium Channel Subunit, Cause Leber Congenital Amaurosis

Reference

Sergouniotis, Panagiotis I., et al. “Recessive Mutations in KCNJ13, Encoding an Inwardly Rectifying Potassium Channel Subunit, Cause Leber Congenital Amaurosis”. The American Journal of Human Genetics, vol. 89, no. 1, June 2011, pp. 183–190, https://doi.org/10.1016/j.ajhg.2011.06.002.

PubMed Reference Number (PMID)

21763485