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Genetic and Clinical Characteristics of Patients With Hereditary Spherocytosis in Hubei Province of China
Hereditary spherocytosis (HS) is an inherited disorder characterized by anemia, splenomegaly, and spherical-shaped erythrocytes, caused by mutations in erythrocyte membrane Protein Genes (ANK1, SPTB, SLC4A1, SPTA1, and EPB42). We investigated molecular spectrum and genotype-phenotype correlation in...
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| Publicado no: | Front Genet |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7461774/ https://ncbi.nlm.nih.gov/pubmed/33014018 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2020.00953 |
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