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

por Khan, Nahid Akhtar, Govindaraj, Periyasamy, Jyothi, Vuskamalla, Meena, Angamuthu K, Thangaraj, Kumarasamy
Publicado 2013

Genome-wide analysis correlates Ayurveda Prakriti

por 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
Publicado 2015