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

Dettagli Bibliografici
Autori principali: Yusuf, IH, Gliem, M, Birtel, J, Muller, PL, Mangold, E, Bolz, H, Issa, PC
Natura: Conference item
Lingua:English
Pubblicazione: Association for Research in Vision and Ophthalmology 2018