Congenital stationary night blindness: an update and review of the disease spectrum in Saudi Arabia-Reference-Cited by-同舟云学术

Congenital stationary night blindness: an update and review of the disease spectrum in Saudi Arabia

Author:

Almutairi Faris¹²,Almeshari Nawaf²,Ahmad Khabir³,Magliyah Moustafa S.¹⁴,Schatz Patrik¹⁵^ORCID

Affiliation:

1. Vitreoretinal Division King Khaled Eye Specialist Hospital Riyadh Saudi Arabia

2. King Khalid University Hospital Riyadh Saudi Arabia

3. Research Department King Khaled Eye Specialist Hospital Riyadh Saudi Arabia

4. Ophthalmology Department Prince Mohammed Medical City AlJouf Saudi Arabia

5. Department of Ophthalmology Clinical Sciences Skane University Hospital Lund University Lund Sweden

Publisher

Wiley

Subject

Ophthalmology,General Medicine

Link

Reference53 articles.

3. A null mutation in CABP4 causes Leber's congenital amaurosis‐like phenotype;Aldahmesh MA;Mol Vis,2010

4. Long‐term follow‐up of retinal function and structure in TRPM1‐associated complete congenital stationary night blindness;Al‐Hujaili H;Mol Vis,2019

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