A carregar...
Sickle Cell Disease—Genetics, Pathophysiology, Clinical Presentation and Treatment
Sickle cell disease (SCD) is a monogenetic disorder due to a single base-pair point mutation in the β-globin gene resulting in the substitution of the amino acid valine for glutamic acid in the β-globin chain. Phenotypic variation in the clinical presentation and disease outcome is a characteristic...
Na minha lista:
| Publicado no: | Int J Neonatal Screen |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2019
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7510211/ https://ncbi.nlm.nih.gov/pubmed/33072979 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijns5020020 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|