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Home  |   Publications  |  Identification of novel mutations in ABCA4 gene: Clinical and Genetic analysis of Indian patients with Stargardt disease

Identification of novel mutations in ABCA4 gene: Clinical and Genetic analysis of Indian patients with Stargardt disease

Rajani Battu, Anshuman Verma, Ramesh Hariharan, Shuba Krishna, Ravi Kiran, Jemima Jacob, Aparna Ganapathy, Vedam L. Ramprasad, Govindasamy Kumaramanickavel, Nallathambi Jeyabalan, and Arkasubhra Ghosh (2015). BioMed Research International, Volume 2015, Article ID 940864..

Stargardt disease (STGD) is the leading cause of juvenile macular degeneration associated with progressive central vision loss, photophobia and color vision abnormalities. The purpose of this study is to describe the clinical and genetic features of Stargardt patients from an Indian cohort.

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