突变
葡萄糖脑苷酶
疾病
杂合子优势
医学
遗传学
病理
生物
等位基因
基因
作者
Rui Zhang,Mei Liu,Xin Wei,Zhongli Gao,Ming Gao,Youguang Guo,Xiaofei Li,Songyun Zhang,Min Shi
标识
DOI:10.7754/clin.lab.2024.240937
摘要
The results show that a heterozygous complex mutation of R496H and L444P in the GBA gene causes the development of GD1. Clinical, enzyme activity-based assays, biological markers, and genetic analysis can significantly improve disease diagnosis and are important for early intervention and GD treatment.
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