Article

Hebbar, Malavika and Harsha Prasada, L. and Das Bhowmik, A. and Trujillano, D. and Shukla, A. and Chakraborti, Shrijeet and Kandaswamy, K.K. and Rolfs, A. and Kamath, N. and Dalal, Ashwin and Bielas, S. and Girisha, K.M. (2016) Homozygous deletion of exons 2 and 3 of NPC2 associated with Niemann-Pick disease type C. American Journal of Medical Genetics Part A, 170 (9). pp. 2486-2489. ISSN 1552-4825

Bidchol, A.M. and Dalal, Ashwin and Trivedi, R. and Shukla, A. and Nampoothiri, S. and Sankar, V.H. and Danda, S. and Gupta, N. and Kabra, M. and Hebbar, S.A. and Bhat, R.Y. and Matta, D. and Ekbote, A.V. and Puri, R.D. and Phadke, S.R. and Gowrishankar, K. and Aggarwal, Shagun and Ranganath, P. and Sharda, S. and Kamate, M. and Datar, C.A. and Bhat, K. and Kamath, N. and Shah, H. and Krishna, S. and Gopinath, P.M. and Verma, I.C. and Nagarajaram, H.A. and Satyamoorthy, K. and Girisha, K.M. (2015) Recurrent and novel GLB1 mutations in India. Gene, 567 (2). pp. 173-181. ISSN 0378-1119