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Glucose‐6‐phosphate dehydrogenase deficiency: not exclusively in males

Glucose‐6‐phosphate (G6PD) deficiency is the most common human enzyme defect, often presenting with neonatal jaundice and/or acute hemolytic anemia, triggered by oxidizing agents. G6PD deficiency is an X‐linked, hereditary disease, mainly affecting men, but should also be considered in females with...

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Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Clin Case Rep
Asıl Yazarlar: van den Broek, Leonie, Heylen, Evelien, van den Akker, Machiel
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: John Wiley and Sons Inc. 2016
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5134135/
https://ncbi.nlm.nih.gov/pubmed/27980749
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.714
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