一名ALG12-CDG患者患有与低ALG12mRNA相关的新型同卵性内基突变
Sandrine Vuillaumier-Barrot1,2, Thierry Dupré1,2, Tiffany Andriantsihoarana1
1Université Paris Cité, INSERM U1149, 16 Rue Henri Huchard, 75018, Paris, France.
Orphanet journal of rare diseases
|February 21, 2025
概括
这项研究确定了ALG12基因中的一种新型内基因变异,导致一种罕见的遗传疾病,即I型糖基化先天性疾病 (CDG-I). 这一发现澄清了患者的诊断,并扩展了对CDG-I.I.已知的突变.
科学领域:
- 生物化学 生物化学
- 遗传学 是一个遗传学.
- 分子生物学分子生物学
背景情况:
- I型血糖代谢先天性乱 (CDG-I) 是一种影响蛋白N-血糖代谢的遗传代谢疾病.
- 缺陷是由于核心寡糖体前体Glc3Man9GlcNAc2-PP-dolichol的合成或转移受损而产生的.
关键词:
在 ALG1212 中.葡萄糖化先天性疾病这是一种多利霍尔结合的寡糖化物.内部变种是一种内部变种.通过N-Glycosylation进行了N-Glycosylation.在RFT1中,RFT1是指RFT1.更多相关视频
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