Genetic profile and mutation spectrum of Leber congenital amaurosis in a larger Indian cohort using high throughput targeted re-sequencing-Reference-Cited by-同舟云学术

Genetic profile and mutation spectrum of Leber congenital amaurosis in a larger Indian cohort using high throughput targeted re-sequencing

Author:

Srikrupa N.N.¹²,Srilekha S.¹,Sen P.³,Arokiasamy T.¹,Meenakshi S.⁴,Bhende M.³,Kapur S.⁵,Soumittra N.¹^ORCID

Affiliation:

1. SNONGC Department of Genetics and Molecular Biology; Vision Research Foundation; Chennai India

2. PhD Scholar; Birla Institute of Technology & Science (BITS); Hyderabad India

3. Department of Vitreo-Retinal Services; Medical Research Foundation; Chennai India

4. Department of Pediatric Ophthalmology; Medical Research Foundation; Chennai India

5. Department of Biological Sciences; Birla Institute of Technology & Science (BITS); Hyderabad India

Funder

Department of Biotechnology , Ministry of Science and Technology

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

Reference37 articles.

1. Amaurosis congenita (Leber);Schappert-Kimmijser;AMA Arch Ophthalmol,1959

Cited by 15 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献