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

Detaylı Bibliyografya
Asıl Yazarlar: Yusuf, IH, Gliem, M, Birtel, J, Muller, PL, Mangold, E, Bolz, H, Issa, PC
Materyal Türü: Conference item
Dil:English
Baskı/Yayın Bilgisi: Association for Research in Vision and Ophthalmology 2018