Gene Expression Analysis of Mevalonate Kinase Deficiency Affected Children Identifies Molecular Signatures Related to Hematopoiesis

Mevalonate kinase deficiency (MKD) is a rare autoinflammatory genetic disorder characterized by recurrent fever attacks and systemic inflammation with potentially severe complications. Although it is recognized that the lack of protein prenylation consequent to mevalonate pathway blockade drives IL1...

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Detalles Bibliográficos
Autores principales: Pisanti, Simona, Citro, Marianna, Abate, Mario, Caputo, Mariella, Martinelli, Rosanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7908123/
https://www.ncbi.nlm.nih.gov/pubmed/33525735
http://dx.doi.org/10.3390/ijerph18031170

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7908123/
https://www.ncbi.nlm.nih.gov/pubmed/33525735
http://dx.doi.org/10.3390/ijerph18031170

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