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An intron c.149-2632T>A change in RHD is associated with aberrant transcription and very weak D phenotype.

Transfusion - 1 Feb 2022

Floch Aline, Vege Sunitha, Berardi Philip, Hannon Judith, Ochoa-Garay Gorka, Lomas-Francis Christine, Westhoff Connie M

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 34936100
DOI: 10.1111/trf.16774

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

An intron c.149-2632T>A change in RHD is associated with aberrant transcription and very weak D phenotype.PMID 34936100Read ↗

The c.254C>A change (p.Ala85Glu) in RHD causing a weak D phenotype.Semantic proximity Read ↗

A novel RHD (c.509T>G, p.Met170Arg) allele shows weakened D expression.Semantic proximity Read ↗

A novel RHD allele, RHD c.56C>G (p.Thr19Arg), with Del phenotype identified in a Chinese family.Semantic proximity Read ↗

A novel RHD allele, RHD*1166delA, with D-negative phenotype identified in a Chinese family.Semantic proximity Read ↗

A new RHD variant allele (RHD Gly339Val) shows weakened D expression compared to RHD Gly339Glu and Gly339Arg mutants.Semantic proximity Read ↗

Novel RHD variant causing RhD negative phenotype identified in a pregnant woman.Semantic proximity Read ↗

A novel RHD allele caused by c.767 C>T mutation was identified in a Chinese individual.Semantic proximity Read ↗

Identification of a novel missense mutation (p.Ser230Asn) in RHD allele in a Chinese individual with partial D phenotype.Semantic proximity Read ↗

New RHD variant alleles.Semantic proximity Read ↗

A novel RHD allele caused by c.687_689delAAG variant.Semantic proximity Read ↗

A novel missense mutation (c.221G>C) in RHD gene identified in a Chinese woman.Semantic proximity Read ↗

Identification of a novel c.94dupA mutation in RHD allele.Semantic proximity Read ↗

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