Multi-OMICS analyses unveil STAT1 as a potential modifier gene in mevalonate kinase deficiency.
多组学分析揭示 STAT1 是甲羟戊酸激酶缺乏症的潜在修饰基因
期刊:Annals of the Rheumatic Diseases
影响因子:20.6
doi:10.1136/annrheumdis-2018-213524
Carapito Raphael, Carapito Christine, Morlon Aurore, Paul Nicodème, Vaca Jacome Alvaro Sebastian, Alsaleh Ghada, Rolli Véronique, Tahar Ouria, Aouadi Ismail, Rompais Magali, Delalande François, Pichot Angélique, Georgel Philippe, Messer Laurent, Sibilia Jean, Cianferani Sarah, Van Dorsselaer Alain, Bahram Seiamak