Clinical phenotype and neuroimaging findings in a French family with hereditary ferritinopathy (FTL498-499InsTC)-Reference-Cited by-同舟云学术

Clinical phenotype and neuroimaging findings in a French family with hereditary ferritinopathy (FTL498-499InsTC)

Published:2009-08-15 Issue:11 Volume:24 Page:1676-1683
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Ory-Magne Fabienne,Brefel-Courbon Christine,Payoux Pierre,Debruxelles Sabrina,Sibon Igor,Goizet Cyril,Labauge Pierre,Menegon Patrice,Uro-Coste Emmanuelle,Ghetti Bernardino,Delisle Marie Bernadetle,Vidal Ruben,Rascol Olivier

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference14 articles.

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

2. Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation;Chinnery;Brain,2007

3. Intracellular ferritin accumulation in neural and extraneural tissue characterizes a neurodegenerative disease associated with a mutation in the ferritin light polypeptide gene;Vidal;J Neuropathol Exp Neurol,2004

4. Hereditary ferritinopathy: a novel mutation, its cellular pathology, and pathogenetic insights;Mancuso;J Neuropathol Exp Neurol,2005

5. Human ferritin gene is assigned to chromosome 19;Caskey;Proc Natl Acad Sci USA,1983

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