References
- Bunker CH, Berson EL, Bromley WC, et al. Prevalence of retinitis pigmentosa in Maine. Am J Ophthalmol 1984;97(3):357–365.
- Sen P, Bhargava A, George R, et al. Prevalence of retinitis pigmentosa in South Indian population aged above 40 years. Ophthalmic Epidemiol 2008;15(4):279–281.
- Adhi MI. Ahmed J. Frequency and clinical presentation of retinal dystrophies: a hospital based study. Pak J Ophthalmol 2002;18(4):106–110.
- Ahlin T, Nichter M, Pillai G. Health insurance in India: what do we know and why is ethnographic research needed. Anthropol Med 2016</b>;23:1,102–124.
- Verma IC. Burden of genetic disorders in India. Indian J Pediatr 2001; 67:893–898.Erratumin: Indian Journal of Pediatrics 2001;68: 25.
- Singh JR. Singh AR and Singh AR. Directory of human genetic services in India—2007. Int J Hum Genet 2010;10:187–192.
- Nirmalan PK, Krishnaiah S, Nutheti R, et al. Consanguinity and eye diseases with a potential genetic etiology. Data from a Prevalence Study in Andhra Pradesh, India. Ophthalmic Epidemiol 2006;13(1):7–13.
- Chakrabarti S, Sarhadi VK, Singh D, et al. Clinical genetic analysis of retinitis pigmentosa in Indian population. Indian J Human Gent 2001;1(2):133–137.
- Ankala A, Tamhankar PM, Valencia CA, Rayam KK. Kumar MM and Hegde MR. Clinical applications and implications of common and founder mutations in Indian subpopulations. Hum Mutat 2015;36:1–10.
- Khan MI, Azam M, Ajmal M, et al. The molecular basis of retinal dystrophies in Pakistan. Genes 2014;5(1):176–195. doi:10.3390/genes5010176.
- Chadda RK, Deb KS. Indian family systems, collectivistic society and psychotherapy. Indian J Psychiatry 2013;55:299–309.
- Rajasimha HK, Shirol PB, Ramamoorthy P, et al. Organization for rare diseases India (ORDI): addressing the challenges and opportunities for the Indian rare diseases’ community. Genet Res (Camb) 2014;96:1–10.