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Neurodegeneration associated with genetic defects in phospholipase A(2)
OBJECTIVE: Mutations in the gene encoding phospholipase A(2) group VI (PLA2G6) are associated with two childhood neurologic disorders: infantile neuroaxonal dystrophy (INAD) and idiopathic neurodegeneration with brain iron accumulation (NBIA). INAD is a severe progressive psychomotor disorder in whi...
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主要な著者: | , , , , , , , , , , , , , , , , , , , , , |
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フォーマット: | Artigo |
言語: | Inglês |
出版事項: |
American Academy of Neurology
2008
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主題: | |
オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2676964/ https://ncbi.nlm.nih.gov/pubmed/18799783 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/01.wnl.0000327094.67726.28 |
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