PLA2G6 gene

Known as: iPLA2beta, NBIA2, PARK14 
This gene plays a role in apoptosis and membrane remodeling.
National Institutes of Health

Papers overview

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2013
2013
Mutations in PLA2G6 gene have variable phenotypic outcome including infantile neuroaxonal dystrophy, atypical neuroaxonal… (More)
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Highly Cited
2012
Highly Cited
2012
The 2 major types of neurodegeneration with brain iron accumulation (NBIA) are the pantothenate kinase type 2 (PANK2)-associated… (More)
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2010
2010
BACKGROUND PLA2G6 is the causative gene for infantile neuroaxonal dystrophy, neurodegeneration associated with brain iron… (More)
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Review
2009
Review
2009
Neurodegeneration with brain iron accumulation (NBIA) describes a group of progressive neurodegenerative disorders characterised… (More)
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2009
2009
BACKGROUND PLA2G6 mutations are known to be responsible for infantile neuroaxonal dystrophy (INAD) and neurodegeneration with… (More)
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2009
2009
BACKGROUND AND PURPOSE Infantile neuroaxonal dystrophy (INAD) is a rare autosomal recessive neurodegenerative disorder. The most… (More)
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Highly Cited
2008
Highly Cited
2008
BACKGROUND Although many recessive loci causing parkinsonism dystonia have been identified, these do not explain all cases of the… (More)
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Highly Cited
2008
Highly Cited
2008
Mutations in the PLA2G6 gene, which encodes group VIA calcium-independent phospholipase A2 (iPLA(2)beta), were recently… (More)
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Highly Cited
2008
Highly Cited
2008
OBJECTIVE Mutations in the gene encoding phospholipase A(2) group VI (PLA2G6) are associated with two childhood neurologic… (More)
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Highly Cited
2006
Highly Cited
2006
Infantile neuroaxonal dystrophy (INAD) is an autosomal recessive progressive neurodegenerative disease that presents within the… (More)
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