A novel c.1937T>C (p.Leu646Pro) missense mutation in a patient with Leber congenital amaurosis. Kaur S, Sukhija J, Kaur A, Srivastava P, et al. J AAPOS 2022 Jan 28. pii: S1091-8531(21)00587.

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Kaur S, Sukhija J, Kaur A, Srivastava P, et al. A novel c.1937T>C (p.Leu646Pro) missense mutation in a patient with Leber congenital amaurosis. J AAPOS 2022 Jan 28. pii: S1091-8531(21)00587.
PMID: 35101627