Llwytho...

Sickle Cell Disease—Genetics, Pathophysiology, Clinical Presentation and Treatment

Sickle cell disease (SCD) is a monogenetic disorder due to a single base-pair point mutation in the β-globin gene resulting in the substitution of the amino acid valine for glutamic acid in the β-globin chain. Phenotypic variation in the clinical presentation and disease outcome is a characteristic...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Int J Neonatal Screen
Prif Awduron: Inusa, Baba P. D., Hsu, Lewis L., Kohli, Neeraj, Patel, Anissa, Ominu-Evbota, Kilali, Anie, Kofi A., Atoyebi, Wale
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: MDPI 2019
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC7510211/
https://ncbi.nlm.nih.gov/pubmed/33072979
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijns5020020
Tagiau: Ychwanegu Tag
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!