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

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون: Yusuf, IH, Gliem, M, Birtel, J, Muller, PL, Mangold, E, Bolz, H, Issa, PC
التنسيق: Conference item
اللغة:English
منشور في: Association for Research in Vision and Ophthalmology 2018

مواد مشابهة