Clinical and genetic diagnosis of thirteen Japanese patients with hereditary spherocytosis

Hereditary spherocytosis is the most frequent cause of hereditary hemolytic anemia and is classified into five subtypes (SPH1-5) according to OMIM. Because the clinical and laboratory features of patients with SPH1-5 are variable, it is difficult to classify these patients into the five subtypes bas...

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Detalles Bibliográficos
Autores principales: Yamamoto, Keiko Shimojima, Utshigisawa, Taiju, Ogura, Hiromi, Aoki, Takako, Kawakami, Takahiro, Ohga, Shoichi, Ohara, Akira, Ito, Etsuro, Yamamoto, Toshiyuki, Kanno, Hitoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8755803/
https://www.ncbi.nlm.nih.gov/pubmed/35022413
http://dx.doi.org/10.1038/s41439-021-00179-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8755803/
https://www.ncbi.nlm.nih.gov/pubmed/35022413
http://dx.doi.org/10.1038/s41439-021-00179-1

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