Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late...
Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism Complex
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Author / Creator
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. and Kumar, Arun
Publisher
United States: Public Library of Science
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Language
English
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Publisher
United States: Public Library of Science
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Contents
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...
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Full title
Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism Complex
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TN_cdi_plos_journals_1790065436
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1790065436
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ISSN
1932-6203
E-ISSN
1932-6203
DOI
10.1371/journal.pone.0155605
