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Number of items: 4.

Journal Article

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 Wed Aug 31 02:49:37 2016 IST.