Article
Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism Complex.
PloS one - 1 Jan 2016
Kapoor Saketh, Shah Mohd Hussain, Singh Nivedita, Rather Mohammad Iqbal, Bhat Vishwanath, Gopinath Sindhura, Bindu Parayil Sankaran, Taly Arun B, Sinha Sanjib, Nagappa Madhu, Bharath Rose Dawn, Mahadevan Anita, Narayanappa Gayathri, Chickabasaviah Yasha T, Kumar Arun
Abstract excerpt
Mutations in PLA2G6 were identified in patients with a spectrum of neurodegenerative conditions, such as infantile neuroaxonal dystrophy (INAD), atypical late-onset neuroaxonal dystrophy (ANAD) and dystonia parkinsonism complex (DPC). However, there is no report on the genetic analysis of families with members affected with INAD, ANAD and DPC from India. Therefore, the main aim of this study was to perform...
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