Defective FA2H leads to a novel form of neurodegeneration with brain iron accumulation (NBIA)-Reference-Cited by-同舟云学术

Defective FA2H leads to a novel form of neurodegeneration with brain iron accumulation (NBIA)

Published:2010-09-17 Issue:5 Volume:68 Page:611-618
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Kruer Michael C.,Paisán-Ruiz Coro,Boddaert Nathalie,Yoon Moon Y.,Hama Hiroko,Gregory Allison,Malandrini Alessandro,Woltjer Randall L.,Munnich Arnold,Gobin Stephanie,Polster Brenda J.,Palmeri Silvia,Edvardson Simon,Hardy John,Houlden Henry,Hayflick Susan J.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference35 articles.

1. Clinical heterogeneity of neurodegeneration with brain iron accumulation (Hallervorden-Spatz syndrome) and pantothenate kinase-associated neurodegeneration;Thomas;Mov Disord,2004

2. Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease;Curtis;Nat Genet,2001

3. Aceruloplasminemia: molecular characterization of this disorder of iron metabolism;Harris;Proc Natl Acad Sci U S A,1995

4. A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome;Zhou;Nat Genet,2001

5. PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron;Morgan;Nat Genet,2006

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