The retinal phenotype associated with the frequent, synonymous c.783G > A mutation in CDHR1

The retinal phenotype associated with the frequent, synonymous c.783G > A mutation in CDHR1

Detalles Bibliográficos
Main Authors: Yusuf, IH, Gliem, M, Birtel, J, Muller, PL, Mangold, E, Bolz, H, Issa, PC
Formato: Conference item
Idioma:English
Publicado: Association for Research in Vision and Ophthalmology 2018

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