Follow-up study of 25 Chinese children withPLA2G6-associated neurodegeneration
Author:
Affiliation:
1. Department of Pediatrics; Peking University First Hospital; Beijing
2. School of Life Sciences; Fudan University; Shanghai; China
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-1331.2012.03856.x/fullpdf
Reference26 articles.
1. Catalytic residues of group VIB calcium-independent phospholipase A2 (iPLA2gamma);Tanaka;Biochem Biophys Res Commun,2004
2. Syndromes of neurodegeneration with brain iron accumulation (NBIA): an update on clinical presentations, histological and genetic underpinnings, and treatment considerations;Schneider;Mov Disord,2012
3. PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron;Morgan;Nat Genet,2006
4. Phenotypic spectrum of neurodegeneration associated with mutations in the PLA2G6 gene (PLAN);Kurian;Neurology,2008
5. Neurodegeneration associated with genetic defects in phospholipase A2;Gregory;Neurology,2008
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