Novel RHD allele with c.487‐2A>G (IVS3‐2A>G) variant causing RhD negative phenotype

Fuente: Wiley Open Access

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Bibliographic Details
Main Authors:	Yuli Zhu, Lihong Jiang, Zhihui Feng, Aiying Wang
Format:	Artículo Open Access
Published:	Wiley 2024
Subjects:	Transfusion
Online Access:	Acceder al recurso
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