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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...
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| Publicado no: | Blood Transfus |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Edizioni SIMTI - SIMTI Servizi Srl
2020
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| Assuntos: | |
| Acesso em linha: | 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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