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Gene therapy for sickle cell disease
BACKGROUND: Sickle cell disease encompasses a group of genetic disorders characterized by the presence of at least one hemoglobin S (Hb S) allele, and a second abnormal allele that could allow abnormal haemoglobin polymerisation leading to a symptomatic disorder. Autosomal recessive disorders (such...
Shranjeno v:
| izdano v: | Cochrane Database Syst Rev |
|---|---|
| Main Authors: | , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
John Wiley & Sons, Ltd
2020
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| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8275984/ https://ncbi.nlm.nih.gov/pubmed/33251574 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/14651858.CD007652.pub7 |
| Oznake: |
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