C19orf12 and FA2H Mutations Are Rare in Italian Patients With Neurodegeneration With Brain Iron Accumulation-Reference-Cited by-同舟云学术

C19orf12 and FA2H Mutations Are Rare in Italian Patients With Neurodegeneration With Brain Iron Accumulation

Published:2012-06 Issue:2 Volume:19 Page:75-81
ISSN:1071-9091
Container-title:Seminars in Pediatric Neurology
language:en
Short-container-title:Seminars in Pediatric Neurology

Author:

Panteghini Celeste,Zorzi Giovanna,Venco Paola,Dusi Sabrina,Reale Chiara,Brunetti Dario,Chiapparini Luisa,Zibordi Federica,Siegel Brigitte,Garavaglia Barbara,Simonati Alessandro,Bertini Enrico,Nardocci Nardo,Tiranti Valeria

Publisher

Elsevier BV

Subject

Neurology (clinical),Pediatrics, Perinatology and Child Health

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