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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).

Singh, Nivedita and Bhat, Vishwanath Kumble and Tiwari, Ankana and Kodaganur, Srinivas G and Tontanahal, Sagar J and Sarda, Astha and Malini, K V and Kumar, Arun (2017) A homozygous mutation in TRIM36 causes autosomal recessive anencephaly in an Indian family. In: HUMAN MOLECULAR GENETICS, 26 (6). pp. 1104-1114.

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.

This list was generated on Wed Oct 16 19:17:01 2019 IST.