Characterization of the l-ferritin variant 460InsA responsible of a hereditary ferritinopathy disorder

Characterization of the l-ferritin variant 460InsA responsible of a hereditary ferritinopathy disorder

Hereditary ferritinopathies are dominant inherited movement disorders associated with extensive alterations of the l-ferritin C-terminus peptide caused by nucleotide insertions in l-ferritin gene (FTL). We describe the characterization of the most common variant, produced by the 460InsA mutations an...

Full description

Bibliographic Details
Main Authors: Anna Cozzi, Paolo Santambrogio, Barbara Corsi, Alessandro Campanella, Paolo Arosio, Sonia Levi
Format: Article
Language:English
Published: Elsevier 2006-09-01
Series:Neurobiology of Disease
Subjects:
Hereditary ferritinopathy
Ferritin
Iron
Oxidative stress
Online Access:http://www.sciencedirect.com/science/article/pii/S0969996106001239

Internet

http://www.sciencedirect.com/science/article/pii/S0969996106001239

Similar Items