PMM2-CDG-:

Tiago Oliveira1, Ricardo Ferraz2,3,4, Luísa Azevedo5,6

  • 1LAQV/REQUIMTE, BioSIM, Department of Biomedicine, Faculty of Medicine, University of Porto, Alameda Prof. Hernâni Monteiro, Porto, Portugal.

概括

胺转基因酶2缺乏症 (PMM2-CDG) 是最常见的N-糖基化乱,呈现出多种不同的基因型和表型. 对41种误解突变的结构分析揭示了基因型-表型相关性,有助于疾病理解和个性化治疗.