RGD Reference Report - Clinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutation. - Rat Genome Database

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Clinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutation.

Authors: Devos, D  Tchofo, PJ  Vuillaume, I  Destee, A  Batey, S  Burn, J  Chinnery, PF 
Citation: Devos D, etal., Brain. 2009 Jun;132(Pt 6):e109. Epub 2008 Oct 14.
RGD ID: 5509860
Pubmed: (View Article at PubMed) PMID:18854324
DOI: Full-text: DOI:10.1093/brain/awn274

Abstract for this paper unavailable

Annotation

Disease Annotations    

Objects Annotated

Genes (Rattus norvegicus)
Ftl1  (ferritin light chain 1)

Genes (Mus musculus)
Ftl1  (ferritin light polypeptide 1)

Genes (Homo sapiens)
FTL  (ferritin light chain)


Additional Information