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Article

Novel A4GALT gene variation with rare p phenotype in a compound heterozygous Chinese individual.

Transfusion - 1 Jan 2021

Chen Qing, Xiao Jianyu, Duan Zhimin, Shi Lili, Huang Chengyin, Li Min

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 33111355
DOI: 10.1111/trf.16163

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Related research

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Research trail→

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Novel A4GALT gene variation with rare p phenotype in a compound heterozygous Chinese individual.PMID 33111355Read ↗

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

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

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

A novel A allele with c.689G>T mutation identified in a Chinese individual.Semantic proximity Read ↗

A novel A allele with c.963_964insC mutation identified in a Chinese individual.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 A allele with c.499G>A mutation identified in a Chinese individual.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 weak A allele with c.27delC in a Chinese individual.Semantic proximity Read ↗

Identification of a novel missense mutation in A allele in a Chinese individual.Semantic proximity Read ↗

Identification of a novel A allele with a missense mutation (c.737A>G) in a Chinese individual with a weak A phenotype.Semantic proximity Read ↗

A novel A allele with the 595C >T mutation identified in a Chinese individual with the Am phenotype.Semantic proximity Read ↗

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