Genetic and mechanistic evaluation for the weak A phenotype in Ael blood type with IVS6 + 5G>A ABO gene mutation

E-ISSN： 1423-0410|108|1|64-71

ISSN： 0042-9007

Source： VOX SANGUINIS, Vol.108, Iss.1, 2015-01, pp. : 64-71

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

A novel mutation of the GATA site in the erythroid cell‐specific regulatory element of the ABO gene in a blood donor with the AmB phenotype

VOX SANGUINIS, Vol. 108, Iss. 4, 2015-05 ,pp. : 425-427

John Wiley & Sons Inc

Access to resources Recommend Favorite

A 3·0‐kb deletion including an erythroid cell‐specific regulatory element in intron 1 of the ABO blood group gene in an individual with the Bm phenotype

VOX SANGUINIS, Vol. 108, Iss. 3, 2015-04 ,pp. : 310-313

John Wiley & Sons Inc

Access to resources Recommend Favorite

Nondeletional α-Thalassemia (α2- IVS-1-116, A>G HBA2): An α2 Gene Point Mutation Detected in an African-American Female for the First Time

Acta Haematologica, Vol. 132, Iss. 1, 2013-12 ,pp. : 22-23

Karger

Access to resources Recommend Favorite

Rapid Detection of the DPYD IVS14+1G>A Mutation for Screening Patients to Prevent Fluorouracil-Related Toxicity

By Bosch Tessa M.

Molecular Diagnosis & Therapy, Vol. 11, Iss. 2, 2007-01 ,pp. : 105-108

Adis International

Access to resources Recommend Favorite

Rapid Detection of the DPYD IVS14+1G>A Mutation for Screening Patients to Prevent Fluorouracil-Related Toxicity

By Lazar Andreas Gründemann Dirk Schömig Edgar

Molecular Diagnosis & Therapy, Vol. 11, Iss. 5, 2007-01 ,pp. : 341-341

Adis International

Access to resources Recommend Favorite