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	1.	Gene symbol: RPE65. Disease: Leber's congenital amaurosis. Accession #Hm0548. [electronic resource] by Gandra, Mamatha Sundaramurthy, Srilekha Kumaramanickavel, Govindasamy Producer: 20070309 In: Human genetics vol. 118 Availability: No items available. Save to lists Add to cart (remove)
	2.	Novel human pathological mutations. Gene symbol: RPE65. Disease: Leber congenital amaurosis. [electronic resource] by Gandra, Mamatha Elamparithi, Anuradha Sundaramurthy, Srilekha Srivatsan, Sripriya Producer: 20110506 In: Human genetics vol. 127 Availability: No items available. Save to lists Add to cart (remove)
	3.	Retinitis pigmentosa: mutation analysis of RHO, PRPF31, RP1, and IMPDH1 genes in patients from India. [electronic resource] by Gandra, Mamatha Anandula, Venkataramana Authiappan, Vidhya Sundaramurthy, Srilekha Raman, Rajiv Bhattacharya, Shomi Govindasamy, Kumaramanickavel Producer: 20080801 In: Molecular vision vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	4.	Homozygosity mapping guided next generation sequencing to identify the causative genetic variation in inherited retinal degenerative diseases. [electronic resource] by Sundaramurthy, Srilekha Swaminathan, Meenakshi Sen, Parveen Arokiasamy, Tharigopala Deshpande, Swati John, Neetha Gadkari, Rupali A Mannan, Ashraf U Soumittra, Nagasamy Producer: 20170406 In: Journal of human genetics vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)