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Number of items: 4.

Journal Article

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).

Nagappa, Madhu and Sinha, Sanjib and Saini, Jitender S and Kallolimath, Pradeep and Singh, Nivedita and Kumar, Arun and Bindu, Parayil S and Taly, Arun B (2016) Non-Wilsonian hepatolenticular degeneration: Clinical and MRI observations in four families from south India. In: JOURNAL OF CLINICAL NEUROSCIENCE, 27 . pp. 91-94.

Kapoor, Saketh and Bindu, Parayil Sankaran and Taly, Arun B. and Sinha, Sanjib and Gayathri, Narayanappa and Rani, S. Vasantha and Chandak, Giriraj Ratan and Kumar, Arun (2012) Genetic analysis of an Indian family with members affected with Waardenburg syndrome and Duchenne muscular dystrophy. In: MOLECULAR VISION, 18 (211-14). pp. 2022-2032.

This list was generated on Mon Oct 26 13:37:40 2020 IST.