Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism Complex

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 w...

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Dades bibliogràfiques
Publicat a:PLoS One
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: Public Library of Science 2016
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4873246/
https://ncbi.nlm.nih.gov/pubmed/27196560
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0155605
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