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Autor:
Neel S. Iyer, Matthew H. Mossayebi, Tracy J. Gao, Lylach Haizler‐Cohen, Daniele Di Mascio, Rodney A. McLaren Jr, Huda B. Al‐Kouatly
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 7, Pp n/a-n/a (2024)
Abstract Background Glucose‐6‐phosphate dehydrogenase (G6PD) deficiency is an X‐linked recessive disorder that predisposes individuals to hemolysis due to an inborn error of metabolism. We performed a systematic literature review to evaluate G6
Externí odkaz:
https://doaj.org/article/1fa8478b3e704473b401189bfd8c3811