Refinement of the X-linked Nonsyndromic High-Grade Myopia LocusMYP1on Xq28 and Exclusion of 13 Known Positional Candidate Genes by Direct Sequencing

Author:

Ratnamala Uppala1,Lyle Robert2,Rawal Rakesh3,Singh Raminder4,Vishnupriya Satti5,Himabindu Pamini5,Rao Vittal6,Aggarwal Somesh7,Paluru Prasuna8,Bartoloni Lucia9,Young Terri L.10,Paoloni-Giacobino Ariane11,Morris Michael A.11,Nath Swapan K.12,Antonarakis Stylianos E.11,Radhakrishna Uppala11

Affiliation:

1. From the Department of Pharmacology, Creighton University, Omaha, Nebraska;

2. the Department of Medical Genetics, Ullevål University Hospital, Oslo, Norway;

3. the Department of Biochemistry, Gujarat Cancer and Research Institute, Civil Hospital, Ahmedabad, India;

4. Anamay Eye Hospital, Ahmedabad, India;

5. the Department of Genetics, Osmania University, Hyderabad, India;

6. the Jagadamba Hospitals, Hyderabad, India;

7. the Western Regional Institute of Ophthalmology, Ahmedabad, India;

8. the Division of Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania;

9. ULSS12 Veneziana, Laboratorio Analisi, Venezia, Italy; the 10Department of Genetic Medicine and Development, University of Geneva Medical School, Geneva, Switzerland; and

10. the Departments of Ophthalmology and 12Pediatrics and Medicine, Duke University Eye Center, Durham, North Carolina;

11. the Department of Genetic Medicine and Development, University of Geneva Medical School, Geneva, Switzerland; and

12. the Arthritis and Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma.

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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