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Beta Thalassemia Major with Gaucher’s Disease: A Rare Entity
Thalassemia is a genetic disorder due to deletion or mutation in the gene for alpha or beta chain of hemoglobin. Gaucher’s disease (GD) is characterized by a deficiency of a lysosomal enzyme, glucocerebrosidase which occurs due to mutations in the GBA1 gene on chromosome 1. Thalassemia and GD have o...
Tallennettuna:
| Julkaisussa: | Cureus |
|---|---|
| Päätekijät: | , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Cureus
2019
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6758988/ https://ncbi.nlm.nih.gov/pubmed/31565589 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7759/cureus.5179 |
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