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Serological and molecular study of a novel B(A) allele with multiple missense mutations / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 20-22, 2021.
Article Dans Chinois | WPRIM | ID: wpr-879514
ABSTRACT
OBJECTIVE@#To explore the molecular basis for an individual suspected as AwB subtype through DNA sequencing.@*METHODS@#ABO serology was carried out with the standard tube method. To identify the ABO gene haplotype, the amplicons of exon 7 were cloned and sequenced.@*RESULTS@#Serological results showed that the forward typing was AwB and the reverse typing was B. Sequencing analysis revealed that the sample has contained an O01 allele in addition with c.297A>G, c.657C>T, c.796C>A, c.803G>C, c.930G>A variants as compared with the A101 allele.@*CONCLUSION@#Through sequencing analysis, the sample with an AwB subtype by serological testing was identified as a novel B(A) phenotype, which was unreported previously.
Sujets)
Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Phénotype / Système ABO de groupes sanguins / Séquence nucléotidique / Exons / Mutation faux-sens / Allèles Type d'étude: Étude pronostique Limites du sujet: Humains langue: Chinois Texte intégral: Chinese Journal of Medical Genetics Année: 2021 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Phénotype / Système ABO de groupes sanguins / Séquence nucléotidique / Exons / Mutation faux-sens / Allèles Type d'étude: Étude pronostique Limites du sujet: Humains langue: Chinois Texte intégral: Chinese Journal of Medical Genetics Année: 2021 Type: Article