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Investigation of nuclear genes involvement in a Mitochondrial Disorder: Leber’s Hereditary Optic Neuropathy

Implementing Organization

Aravind Medical Research Foundation
Principal Investigator
Dr. Sundaresan Periasamy
Senior Scientist
|
Aravind Medical Research Foundation
CO-Principal Investigator
Dr. Mahesh Kumar
Aravind Medical Research Foundation

About

Mitochondrial complex I deficiency, a genetic disorder causing lung cancer, is linked to environmental factors and environmental factors. Autosomal recessive mitochondrial complex I deficiency (MCIDN) is responsible for 23% of childhood respiratory chain deficiency cases. A study found that 56% of LHON patients have primary and secondary mitochondrial DNA mutations, while the disease progression remains unknown.

Related Research

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Funding Organization
Funding Organization
Science and Engineering Research Board (SERB), New Delhi
Quick Information
Area of Research
Life Sciences & Biotechnology
Focus Area
Genetics
Start Year
2023
End Year
2025
Sanction Amount
₹ 33.56 L
Status
Completed
Contact
sundar@aravind.org
Output
No. of Research Paper
00
Technologies (If Any)
00
No. of PhD Produced
00
No. of Patents
Filed : 00
Grant : 00
Disclaimer: Information available on this portal is sourced from various organizations and is provided for informational purposes only. Users are advised to verify details from the respective official sources.
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