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

Transfusion - 1 Apr 2024

Mo Chunyan, Jia Shuangshuang, Luo Guangping, Ji Yanli

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PMID: 38501748
DOI: 10.1111/trf.17795

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Identification of a novel A4GALT*299A allele associated with the rare p phenotype in one Chinese family.PMID 38501748Read ↗

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

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

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