Items where Author is "Jyothi, Vuskamalla"

Article

Paramasivam, Arumugam ; Meena, Angamuthu Kannan ; Pedaparthi, Lalitha ; Jyothi, Vuskamalla ; Uppin, Megha S. ; Jabeen, Shaikh Afshan ; Sundaram, Challa ; Thangaraj, Kumarasamy (2016) Novel mutation in C10orf2 associated with multiple mtDNA deletions, chronic progressive external ophthalmoplegia and premature aging Mitochondrion, 26 . pp. 81-85. ISSN 1567-7249

Govindaraj, Periyasamy ; Nizamuddin, Sheikh ; Sharath, Anugula ; Jyothi, Vuskamalla ; Rotti, Harish ; Raval, Ritu ; Nayak, Jayakrishna ; Bhat, Balakrishna K. ; Prasanna, B. V. ; Shintre, Pooja ; Sule, Mayura ; Joshi, Kalpana S. ; Dedge, Amrish P. ; Bharadwaj, Ramachandra ; Gangadharan, G. G. ; Nair, Sreekumaran ; Gopinath, Puthiya M. ; Patwardhan, Bhushan ; Kondaiah, Paturu ; Satyamoorthy, Kapaettu ; Valiathan, Marthanda Varma Sankaran ; Thangaraj, Kumarasamy (2015) Genome-wide analysis correlates Ayurveda Prakriti Scientific Reports, 5 . pp. Article ID 15786-12 pages. ISSN 2045-2322

Govindaraj, Periyasamy ; Khan, Nahid Akhtar ; Rani, Bindu ; Rani, Deepa Selvi ; Selvaraj, Priyadharshini ; Jyothi, Vuskamalla ; Bahl, Ajay ; Narasimhan, Calambur ; Rakshak, Dharma ; Premkumar, Kumpati ; Khullar, Madhu ; Thangaraj, Kumarasamy (2014) Mitochondrial DNA variations associated with hypertrophic cardiomyopathy Mitochondrion, 16 . pp. 65-72. ISSN 1567-7249

Khan, Nahid Akhtar ; Govindaraj, Periyasamy ; Jyothi, Vuskamalla ; Meena, Angamuthu K. ; Thangaraj, Kumarasamy (2013) 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 Molecular Vision, 19 . pp. 1282-1289. ISSN 1090-0535