<i>RPE65</i> mutations in Leber congenital amaurosis, early-onset severe retinal dystrophy, and retinitis pigmentosa from a tertiary eye care center in India-Reference-Cited by-同舟云学术

RPE65 mutations in Leber congenital amaurosis, early-onset severe retinal dystrophy, and retinitis pigmentosa from a tertiary eye care center in India

Published:2024-02-07 Issue:3 Volume:45 Page:303-312
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Parameswarappa Deepika C.¹,Bagga Deepak Kumar²,Upadhyaya Abhishek¹,Balasubramanian Jeyapoorani³,Pochaboina Venkatesh³,Muthineni Vani⁴,Jalali Subhadra¹,Kannabiran Chitra⁴

Affiliation:

1. Srimati Kanuri Santhamma Center for Vitreoretinal Diseases, Anant Bajaj Retina Institute, Kallam Anji Reddy Campus, L V Prasad Eye Institute, Hyderabad, India

2. Meera and L B Deshpande Centre for Sight Enhancement, Institute for Vision Rehabilitation, L V Prasad Eye Institute, Hyderabad, India

3. Department of Clinical Genetics and Genetic Counseling, L V Prasad Eye Institute, Hyderabad, India

4. Kallam Anji Reddy Molecular Genetics Laboratory, L V Prasad Eye Institute, Hyderabad, India

Funder

Hyderabad Eye Research Foundation

Publisher

Informa UK Limited

Link

https://www.tandfonline.com/doi/pdf/10.1080/13816810.2024.2309559

Reference35 articles.

1. Leber Congenital Amaurosis

2. Leber Congenital Amaurosis

3. Leber congenital amaurosis/early-onset severe retinal dystrophy: clinical features, molecular genetics and therapeutic interventions

4. Retinitis pigmentosa

5. Retinitis Pigmentosa

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