Associated Papers
PLA2G6-associated neurodegeneration presenting as a complicated form of hereditary spastic paraplegia.
Koh K et al.
Journal of Human Genetics, 2019
Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism Complex.
Kapoor S et al.
Plos One, 2016
27196560 (PubMed )
Supplement: pone.0155605.s001.pdf
Select a paper to view details