New spastic paraplegia phenotype associated to mutation of NFU1

Recently an early onset lethal encephalopathy has been described in relation to mutations of NFU1, one of the genes involved in iron-sulfur cluster metabolism. We report a new NFU1 mutated patient presenting with a milder phenotype characterized by a later onset, a slowly progressive spastic parapar...

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Detalles Bibliográficos
Autores principales: Tonduti, Davide, Dorboz, Imen, Imbard, Apolline, Slama, Abdelhamid, Boutron, Audrey, Pichard, Samia, Elmaleh, Monique, Vallée, Louis, Benoist, Jean François, Ogier, Heléne, Boespflug-Tanguy, Odile
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Letter to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4333890/
https://www.ncbi.nlm.nih.gov/pubmed/25758857
http://dx.doi.org/10.1186/s13023-015-0237-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4333890/
https://www.ncbi.nlm.nih.gov/pubmed/25758857
http://dx.doi.org/10.1186/s13023-015-0237-6

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