G gamma beta+ hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the G gamma gene.

Hereditary persistence of fetal hemoglobin (HPFH) is a benign condition in which the normal shutoff of fetal hemoglobin (Hb F) production fails to occur. In the G gamma beta+ type of HPFH, erythrocytes of adult heterozygotes contain approximately equal to 20% Hb F, which is almost exclusively of the...

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Vydáno v:	Proc Natl Acad Sci U S A
Hlavní autoři:	Collins, F S, Stoeckert, C J, Serjeant, G R, Forget, B G, Weissman, S M
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	National Academy of Sciences 1984
Témata:	Research Article
On-line přístup:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC391598/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6205403/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.81.15.4894
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