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Number of items: 6.

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).

Yadav, Ravi and Kapoor, Saketh and Madhukar, Mayank and Naduthota, Rajini M and Kumar, Arun and Pal, Pramod Kumar (2018) Genetic analysis of the glucocerebrosidase gene in South Indian patients with Parkinson's disease. In: NEUROLOGY INDIA, 66 (6). pp. 1649-1654.

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).

Netravathi, Manjunath and Kumari, Renu and Kapoor, Saketh and Dakle, Pushkar and Dwivedi, Manish Kumar and Roy, Sumitabho Deb and Pandey, Paritosh and Saini, Jitender and Ramakrishna, Anil and Navalli, Devaraddi and Satishchandra, Parthasarathy and Pal, Pramod Kumar and Kumar, Arun and Faruq, Mohammed (2015) Whole exome sequencing in an Indian family links Coats plus syndrome and dextrocardia with a homozygous novel CTC1 and a rare HES7 variation. In: BMC MEDICAL GENETICS, 16 .

Kodaganur, Srinivas Gopinath and Kapoor, Saketh and Veerappa, Avinash M and Tontanahal, Sagar Jagannath and Sarda, Astha and Yathish, S and Prakash, Ravi D and Kumar, Arun (2013) Mutation analysis of the SLC4A11 gene in Indian families with congenital hereditary endothelial dystrophy 2 and a review of the literature. In: Molecular Vision, 19 . pp. 1694-1706.

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 Fri Mar 29 06:50:07 2024 IST.