GNAT1Associated with Autosomal Recessive Congenital Stationary Night Blindness
Investigative Ophthalmology & Visual Science2011Vol. 53(3), pp. 1353–1353
Citations Over TimeTop 22% of 2011 papers
Muhammad Asif Naeem, Venkata Ramana Murthy Chavali, Shahbaz Ali, Muhammad Iqbal, Saima Riazuddin, Shaheen N. Khan, Tayyab Husnaın, Paul A. Sieving, Radha Ayyagari, Sheikh Riazuddin, J. Fielding Hejtmancik, Sheikh Riazuddin
Abstract
These data suggest that a homozygous missense mutation in GNAT1 is associated with autosomal recessive stationary night blindness.
Related Papers
- Profile of blindness in Nepal: a hospital based study.(2005)
- → Sightsavers International(2021)2 cited
- → CAUSES OF BLINDNESS IN PENNSYLVANIA(1936)9 cited
- The strategy of prevention of blindness.(1997)
- Study: 123 million+ lost workdays per year caused by blindness or eye diseases(2014)