טוען...
Two novel mutations p. L319V and p. L91P in ABO glycosyltransferases lead to A(el) and B(el) phenotypes
BACKGROUND: Mutations of the 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 their mechanisms that caused A(el) and B(el) phenotypes. MATERIALS AND METHODS: The ABO phenoty...
שמור ב:
| הוצא לאור ב: | Blood Transfus |
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| Main Authors: | , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Edizioni SIMTI - SIMTI Servizi Srl
2020
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7605879/ https://ncbi.nlm.nih.gov/pubmed/32281923 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2450/2020.008-20 |
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