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Identification of a novel P1PK allele (A4GALT*c.1-504_1044del1548) in two Chinese sisters with a history of recurrent spontaneous abortion.

Transfusion - 1 Sept 2022

Jia Shuangshuang, Li Si, Liao Zhijian, Mo Chunyan, Fang Qun, Luo Guangping, Ji Yanli

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PMID: 35929100
DOI: 10.1111/trf.17050

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Identification of a novel P1PK allele (A4GALT*c.1-504_1044del1548) in two Chinese sisters with a history of recurrent spontaneous abortion.PMID 35929100Read ↗

A novel P1PK allele in two Bangladeshi sisters with a history of spontaneous abortion: A4GALT*02N(951C).Semantic proximity Read ↗

Novel A4GALT Variants Cause Rare p Phenotype and Recurrent Pregnancy Loss in a Chinese Individual.Semantic proximity Read ↗

Identification of a novel A4GALT*299A allele associated with the rare p phenotype in one Chinese family.Semantic proximity Read ↗

A new allele with 303 base pairs insertion in B3GALT1 gene identified in an individual with P1 k phenotype.Semantic proximity Read ↗

A novel mutation in A4GALT was identified in a Chinese individual with p phenotype.Semantic proximity Read ↗

Novel A4GALT gene variation with rare p phenotype in a Chinese family.Semantic proximity Read ↗

Anti-Tja (PP1Pk) : Rare cause of recurrent early abortion.Semantic proximity Read ↗

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