Mutations in <i>CERKL</i> and <i>RP1</i> cause retinitis pigmentosa in Pakistani families.

Mutations in CERKL and RP1 cause retinitis pigmentosa in Pakistani families.

Nadeem, Raheela; Kabir, Firoz; Li, Jiali; Gradstein, Libe; Jiao, Xiaodong; Rauf, Bushra; Naeem, Muhammad Asif; Assir, Muhammad Zaman; Riazuddin, Sheikh; Ayyagari, Radha; Hejtmancik, J Fielding; Riazuddin, S Amer.

Afiliación

Nadeem R; 1National Centre of Excellence in Molecular Biology, University of the Punjab, Lahore, 53700 Pakistan.
Kabir F; 2The Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21287 USA.
Li J; 3Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, MD 20892 USA.
Gradstein L; 4Department of Ophthalmology, Zhujiang Hospital, Southern Medical University, Guangzhou, 515282 China.
Jiao X; 3Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, MD 20892 USA.
Rauf B; 3Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, MD 20892 USA.
Naeem MA; 1National Centre of Excellence in Molecular Biology, University of the Punjab, Lahore, 53700 Pakistan.
Assir MZ; 1National Centre of Excellence in Molecular Biology, University of the Punjab, Lahore, 53700 Pakistan.
Riazuddin S; Allama Iqbal Medical College, University of Health Sciences, Lahore, 54550 Pakistan.
Ayyagari R; 1National Centre of Excellence in Molecular Biology, University of the Punjab, Lahore, 53700 Pakistan.
Hejtmancik JF; Allama Iqbal Medical College, University of Health Sciences, Lahore, 54550 Pakistan.
Riazuddin SA; 6Shiley Eye Institute, University of California San Diego, La Jolla, CA 92093 USA.