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Serological weak D phenotype caused by a novel RHD variant allele with a nucleotide change (c. 283G >T)

Fuente: Wiley Open Access

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Dettagli Bibliografici
Autori principali:	Jue Hou, Yuwei Zhao, Meng Li, Xue Chen
Natura:	Artículo Open Access
Pubblicazione:	Wiley 2026
Soggetti:	Transfusion
Accesso online:	Acceder al recurso
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