First Report of Known Rare Rhnull Phenotype Individuals in Iran

Rhnull phenotype is a rare blood group with a frequency of approximately 1 in 6 million individuals, transmitted via an autosomal recessive mode. It is characterized by the weak (Rhmod) or lack (Rhnull) of expression of all Rh antigens on the red cells. The clinical significance of its assessment is...

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Detalles Bibliográficos
Autores principales: Shahverdi, Ehsan, Moghaddam, Mostafa, Abolghasemi, Hassan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences, Hematology-Oncology and Stem Cell Transplantation Research Center 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305262/
https://www.ncbi.nlm.nih.gov/pubmed/30595819

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