Llwytho...

Paroxysmal nocturnal hemoglobinuria caused by CN-LOH of constitutional PIGB mutation and 70-kbp microdeletion on 15q

Paroxysmal nocturnal hemoglobinuria (PNH) is a rare hematopoietic stem cell (HSC) disorder characterized by defective synthesis of the glycosylphosphatidylinositol (GPI) anchors as a result of somatic mutations in the X-linked PIGA gene. The disease is acquired. No constitutional PNH has been descri...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Blood Adv
Prif Awduron: Langemeijer, Saskia, Schaap, Charlotte, Preijers, Frank, Jansen, Joop H., Blijlevens, Nicole, Inoue, Norimitsu, Muus, Petra, Kinoshita, Taroh, Murakami, Yoshiko
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: American Society of Hematology 2020
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC7686886/
https://ncbi.nlm.nih.gov/pubmed/33216889
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/bloodadvances.2020002210
Tagiau: Ychwanegu Tag
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!