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Profile of crizanlizumab and its potential in the prevention of pain crises in sickle cell disease: evidence to date

Sickle cell disease (SCD) is one of the most common inherited blood disorders globally. It is a grouping of autosomal recessive genetic disorders identified by a genetic mutation that replaces glutamic acid with valine at the sixth amino acid on the hemoglobin β-globin chain. Millions of people arou...

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Dades bibliogràfiques
Publicat a:J Blood Med
Autors principals: Riley, Tanya R, Riley, Treavor T
Format: Artigo
Idioma:Inglês
Publicat: Dove 2019
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6720158/
https://ncbi.nlm.nih.gov/pubmed/31507334
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/JBM.S191423
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