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Novel Variant of the SLC4A1 Gene Associated with Hereditary Spherocytosis

Hereditary spherocytosis (HS) refers to the group of the most frequently occurring non-immune hereditary hemolytic anemia in people of Caucasian central or northern European ancestry. HS is mainly associated with pathogenic variants of genes encoding defects in five membrane proteins, including anio...

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Detalles Bibliográficos
Autores principales:	Bogusławska, Dżamila M., Kraszewski, Sebastian, Skulski, Michał, Potoczek, Stanisław, Kuliczkowski, Kazimierz, Sikorski, Aleksander F.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2023
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10045460/ https://www.ncbi.nlm.nih.gov/pubmed/36979763 http://dx.doi.org/10.3390/biomedicines11030784

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