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Phenotype and Genotype of Cis-AB Family in Chonnam Area / 대한수혈학회지
Article in Korean | WPRIM (Western Pacific) | ID: wpr-7236
Responsible library: WPRO
ABSTRACT

BACKGROUND:

Cis-AB is a rare blood ABO with unusual inheritance on the same chromosome that result from a point mutation. It is relatively common in Korean and Japanese populations. We analyzed serological and molecular genetic characteristics of the family with cis-AB who had visited Chonnam National University Hospital (CNUH) for 10 years. MATERIAL AND

METHODS:

The subjects of this study comprised 88 samples derived from cis-AB family of 17 propositi with A2B3 phenotype diagnosed at CNUH between January 1993 and May 2002. Serologic tests for cis-AB were performed in detail on the ABO antigens of 49 samples, polymerase chain reaction - restriction fragment length polymorphism (PCR-RFLP) method for cis-AB genotyping was additionally performed in peripheral blood DNA samples from 19 cases.

RESULTS:

The phenotypes of 49 cases were composed of 39 cases of A2B3, 7 of A2B, 2 of A1B3 and 1 of A1. ABO genotype on the blood samples from 19 cis-AB cases showed 11 cases of cis-AB/O with phenotype A2B3, 6 of cis-AB/B with phenotype A2B, 1 of cis-AB/A with phenotype A1B3 and 1 of cis-AB/A with phenotype A1.

CONCLUSIONS:

These data demonstrated that the most frequent type of cis-AB cases in Chonnam area was cis-AB/O with phenotype A2B3 and a case of cis-AB/A with unusual A1 phenotype was found.
Subject(s)

Full text: Available Database: WPRIM (Western Pacific) Main subject: Phenotype / Wills / Polymorphism, Restriction Fragment Length / DNA / Serologic Tests / Polymerase Chain Reaction / Point Mutation / Asian People / Genotype / Molecular Biology Type of study: Diagnostic study Limits: Humans Language: Korean Journal: Korean Journal of Blood Transfusion Year: 2002 Document type: Article
Full text: Available Database: WPRIM (Western Pacific) Main subject: Phenotype / Wills / Polymorphism, Restriction Fragment Length / DNA / Serologic Tests / Polymerase Chain Reaction / Point Mutation / Asian People / Genotype / Molecular Biology Type of study: Diagnostic study Limits: Humans Language: Korean Journal: Korean Journal of Blood Transfusion Year: 2002 Document type: Article
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