Molecular genetic analysis of two novel ABO∗A alleles causing Ax phenotype in Chinese
Background: Mutations of ABO gene may cause the dysfunction of ABO glycosyltransferase (GT) that can result in weak ABO phenotypes. Here, we identified two novel weak ABO subgroup alleles and explored the mechanism that caused Ax phenotype. Materials and methods: The ABO phenotyping and genotyping w...
Salvato in:
| Autori principali: | , , , , , , , , |
|---|---|
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Elsevier
2025-09-01
|
| Serie: | Journal of the Formosan Medical Association |
| Soggetti: | |
| Accesso online: | http://www.sciencedirect.com/science/article/pii/S0929664624004066 |
| Tags: |
Nessun Tag, puoi essere il primo ad aggiungerne!!
|
