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	1.	Co-occurrence of m.1555A>G and m.11778G>A mitochondrial DNA mutations in two Indian families with strikingly different clinical penetrance of Leber hereditary optic neuropathy. [electronic resource] by Khan, Nahid Akhtar Govindaraj, Periyasamy Jyothi, Vuskamalla Meena, Angamuthu K Thangaraj, Kumarasamy Producer: 20130924 In: Molecular vision vol. 19 Availability: No items available. Save to lists Add to cart (remove)
	2.	Homozygous R627W mutations in POLG cause mitochondrial DNA depletion leading to encephalopathy, seizures and stroke-like episodes. [electronic resource] by Paramasivam, Arumugam Venkatapathi, Challa Sandeep, Gampa Meena, Angamuthu K Uppin, Megha S Mohapatra, Swati Pitceathly, Robert D S Thangaraj, Kumarasamy Producer: 20200511 In: Mitochondrion vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Haplogroup heterogeneity of LHON patients carrying the m.14484T>C mutation in India. [electronic resource] by Khan, Nahid Akhtar Govindaraj, Periyasamy Soumittra, Nagasamy Srilekha, Sundaramoorthy Ambika, Selvakumar Vanniarajan, Ayyasamy Meena, Angamuthu K Uppin, Megha S Sundaram, Challa Taly, Arun B Bindu, Parayil Sankaran Gayathri, Narayanappa Thangaraj, Kumarasamy Producer: 20130812 In: Investigative ophthalmology & visual science vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)