Transforming growth factor beta‐induced p.(L558P) variant is associated with autosomal dominant lattice corneal dystrophy type IV in a large cohort of Spanish patients.

Autor: Campos‐Mollo, Ezequiel1,2 (AUTHOR), Varela‐Conde, Yago3 (AUTHOR), Arriola‐Villalobos, Pedro2,4,5 (AUTHOR), Cabrera‐Beyrouti, Rubén6 (AUTHOR), Benítez‐del‐Castillo, José‐Manuel2,4,5,7,8 (AUTHOR), Maldonado, Miguel J.2,9 (AUTHOR) maldonado@ioba.med.uva.es, Escribano, Julio2,10 (AUTHOR) julio.escribano@uclm.es
Zdroj: Clinical & Experimental Ophthalmology. Sep2019, Vol. 47 Issue 7, p871-880. 10p.
Databáze: Academic Search Ultimate
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