Dual phenotype: co-occurring Leber congenital amaurosis and familial exudative vitreoretinopathy: a case report.

Autor: Miraldi Utz, Virginia1,2 (AUTHOR), Ebert, Jared J.2 (AUTHOR), Brightman, Diana S.3 (AUTHOR), Simpson, Brittany N.3,4 (AUTHOR), Benoit, Stefanie4,5 (AUTHOR), Sisk, Robert A.1,2,6 (AUTHOR) rsisk@cvphealth.com
Zdroj: Ophthalmic Genetics. Feb2023, Vol. 44 Issue 1, p89-92. 4p.
Databáze: Academic Search Ultimate
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