Sree Chitra Tirunal Institute for Medical Sciences & Technology, Trivandrum
(An Institute of National Importance under Govt. of India)
Browsing by Subject Genetics & Heredity
Showing results 1 to 5 of 5
| Issue Date | Title | Author(s) |
| 2010 | A locus for juvenile myoclonic epilepsy maps to 2q33-q36 | Ratnapriya, R; Vijai, J; Kadandale, JS; Iyer, RS; Radhakrishnan, K; Anand, A |
| 2003 | Absence of GABRA1 Ala322Asp mutation in juvenile myoclonic epilepsy families from India | Kapoor, A; Vijai, J; Ravishankar, HM; Satishchandra, P; Radhakrishnan, K; Anand, A |
| 2013 | Major vault protein (MVP) gene polymorphisms and drug resistance in mesial temporal lobe epilepsy with hippocampal sclerosis (vol 526, pg 449, 2013) | Balan, S; Radha, SK; Sathyan, S; Vijai, J; Banerjee, M; Radhakrishnan, K |
| 2005 | Protective and susceptibility effects of hSKCa3 allelic variants on juvenile myoclonic epilepsy | Vijai, J; Kapoor, A; Ravishankar, HM; Cherian, PJ; Kuruttukulam, G; Rajendran, B; Sridharan, R; Rangan, G; Girija, AS; Jayalakshmi, S; Mohandas, S; Mani, KS; Radhakrishnan, K; Anand, A |
| 2011 | Spinocerebellar ataxia type 17 in Indian patients: two rare cases of homozygous expansions | Hire, RR; Katrak, SM; Vaidya, S; Radhakrishnan, K; Seshadri, M |
