A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy-Reference-Cited by-同舟云学术

A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy

Published:2017-10 Issue: Volume:381 Page:209-212
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Iannello Grazia,Graziano Claudio,Cenacchi Giovanna,Cordelli Duccio Maria,Zuntini Roberta,Papa Valentina,Magistà Anna Maria,Gagliardi Monica,Procopio Radha,Quattrone Aldo,Annesi Grazia

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference28 articles.

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4. Neurodegeneration associated with genetic defects in phospholipase A(2);Gregory;Neurology,2008

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

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