A case of McLeod syndrome caused by a nonsense variation c.942G>A in the XK gene: A case report

McLeod syndrome is a rare XK gene-related progressive, debilitating disease involving multiple systems. The blood group phenotypes in McLeod syndrome patients usually display the Kx antigen loss and a decrease in the Kell blood group system antigen expression. This paper describes a 41-year-old male...

Descripción completa

Detalles Bibliográficos
Autores principales: Ying, Yanling, Yu, Shifang, Zhang, Jingjing, He, Ji, Xu, Xianguo, Hong, Xiaozhen, Zhu, Faming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9929429/
https://www.ncbi.nlm.nih.gov/pubmed/36816020
http://dx.doi.org/10.3389/fgene.2023.1073139

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9929429/
https://www.ncbi.nlm.nih.gov/pubmed/36816020
http://dx.doi.org/10.3389/fgene.2023.1073139

Ejemplares similares