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Una cura per Elena, unica affetta in Italia dalla malattia rara NUPBL. La mamma lancia una campagna per aiutare la ricerca - Articolo21
NUBPL Foundation - September 15-21 is Mitochondrial Disease Awareness Week to educate and increase awareness about mitochondrial disease. This week we want to introduce you to a few mitochondrial disease patients diagnosed
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Fundraiser for AMMeC Malattie Metaboliche Congenite by Andreea @ildiariodiunamammarara : "Il sorriso di Elena"
![NUBPL mitochondrial disease: new patients and review of the genetic and clinical spectrum | Journal of Medical Genetics NUBPL mitochondrial disease: new patients and review of the genetic and clinical spectrum | Journal of Medical Genetics](https://jmg.bmj.com/content/jmedgenet/58/5/314/F3.large.jpg)
NUBPL mitochondrial disease: new patients and review of the genetic and clinical spectrum | Journal of Medical Genetics
![Father fighting for daughter's life is nominated for Eagle Rare Life Award | MadSocial | richmondregister.com Father fighting for daughter's life is nominated for Eagle Rare Life Award | MadSocial | richmondregister.com](https://bloximages.chicago2.vip.townnews.com/richmondregister.com/content/tncms/assets/v3/editorial/a/bc/abc7a6e1-11ae-5418-b6f7-cd78a2246dbf/5bfc7b1702c6c.image.jpg)