GNAT1Associated with Autosomal Recessive Congenital Stationary Night Blindness | Zendy

Muhammad Asif Naeem | Zendy; Venkata Ramana Murthy Chavali | Zendy; Shahbaz Ali | Zendy; Muhammad Iqbal | Zendy; Saima Riazuddin | Zendy; Shaheen N. Khan | Zendy; Tayyab Husnain | Zendy; Paul A. Sieving | Zendy; Radha Ayyagari | Zendy; Sheikh Riazuddin | Zendy; J. Fielding Hejtmancik | Zendy

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GNAT1Associated with Autosomal Recessive Congenital Stationary Night Blindness

Author(s) -

Muhammad Asif Naeem,

Venkata Ramana Murthy Chavali,

Shahbaz Ali,

Muhammad Iqbal,

Saima Riazuddin,

Shaheen N. Khan,

Tayyab Husnain,

Paul A. Sieving,

Radha Ayyagari,

Sheikh Riazuddin,

J. Fielding Hejtmancik

Publication year - 2011

Publication title -

investigative ophthalmology and visual science

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 1.935

H-Index - 218

eISSN - 1552-5783

pISSN - 0146-0404

DOI - 10.1167/iovs.11-8026

Subject(s) - blindness , medicine , ophthalmology , genetics , pediatrics , optometry , biology

Congenital stationary night blindness is a nonprogressive retinal disorder manifesting as impaired night vision and is generally associated with other ocular symptoms, such as nystagmus, myopia, and strabismus. This study was conducted to further investigate the genetic basis of CSNB in a consanguineous Pakistani family.

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