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

Fuente: Wiley Open Access

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Bibliographic Details
Main Authors:	Hongjuan Lyu, Kun Wang, Zhihui Feng, Tao Xu
Format:	Artículo Open Access
Published:	Wiley 2024
Subjects:	Transfusion
Online Access:	Acceder al recurso
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