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[A rare p phenotype caused by a 26-bp deletion in α 1,4-galactosyltransferase gene].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics - 1 Jun 2013

Xu Xianguo, Hong Xiaozhen, Ma Kairong, Lan Xiaofei, Chen Shu, Liu Ying, Ying Yanling, Zhu Faming, Lv Hangjun

Abstract excerpt

OBJECTIVE: To delineate serological features and genetic basis for a rare p phenotype of P1Pk blood group system found in a Chinese individual. METHODS: Serological assaying was carried out for a proband with unexpected antibody found in his serum using specific antibodies and panel cells. Coding regions and flanking introns of α 1,4-galactosyltransferase gene (A4GALT) associated with the p phenotype were...

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Identifiers

PMID: 23744321
DOI: 10.3760/cma.j.issn.1003-9406.2013.03.013

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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