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Singh, Nivedita and Kallollimath, Pradeep and Shah, Mohd Hussain and Kapoor, Saketh and Bhat, Vishwanath Kumble and Viswanathan, Lakshminarayanapuram Gopal and Nagappa, Madhu and Bindu, Parayil S and Taly, Arun B and Sinha, Sanjib and Kumar, Arun (2019) Genetic analysis of ATP7B in 102 south Indian families with Wilson disease. In: PLOS ONE, 14 (5).
Kapoor, Saketh and Shah, Mohd Hussain and Singh, Nivedita and Rather, Mohammad Iqbal and Bhat, Vishwanath and Gopinath, Sindhura and Bindu, Parayil Sankaran and Taly, Arun B and Sinha, Sanjib and Nagappa, Madhu and Bharath, Rose Dawn and Mahadevan, Anita and Narayanappa, Gayathri and Chickabasaviah, Yasha T and Kumar, Arun (2016) Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism Complex. In: PLOS ONE, 11 (5).
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.
