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Shah, Mohd Hussain and Bhat, Vishwanath and Shetty, Jyoti S and Kumar, Arun (2014) Whole exome sequencing identifies a novel splice-site mutation in ADAMTS17 in an Indian family with Weill-Marchesani syndrome. In: MOLECULAR VISION, 20 . pp. 790-796.
Kumar, Arun and Duvvari, Maheswara R and Prabhakaran, Venkatesh C and Shetty, Jyoti S and Murthy, Gowri J and Blanton, Susan Halloran (2010) A homozygous mutation in LTBP2 causes isolated microspherophakia. In: Human Genetics, 128 (4). pp. 365-371.
Kumar, Arun and Basavaraj, Manjunath G and Gupta, Santosh K and Qamar, Imteyaz and Ali, Abdullah Mahmood and Bajaj, Vineeta and Ramesh, TK and Prakash, Ravi D and Shetty, Jyoti S and Dorairaj, Syril K (2007) Role of CYP1B1, MYOC, OPTN and OPTC genes in adult-onset primary open-angle glaucoma: predominance of CYP1B1 mutations in Indian patients. In: Molecular Vision, 13 (73). pp. 667-676.
