Work

Genetic Survey of the Primary Mitochondrial Mutations along with Clinical Correlation in suspected Leber Hereditary Optic Neuropathy (LHON) patients from an Indian Cohort

Year: 2018

Type: article

Source: Investigative Ophthalmology & Visual Science

Authors: Srilekha Sundaramurthy, Jayaprakash Mani, Vidhya Dharani, Soumittra Nagasamy, Sripriya Sarangapani, Sinnakaruppan Mathavan, Ambika Selvakumar

Institutions: Sankara Nethralaya, Vision Research Foundation

Language: English

Topic: Mitochondrial Function and Pathology

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: gold

Estimated APC paid: $1,850

OpenAlex ID: W2993596440

FWCI:

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