Locus assignment of alpha-globin structural mutations by hybrid-selected translation.

The two human alpha-globin genes, alpha 1 and alpha 2 located 3.4 kilobases apart on chromosome 16, encode identical alpha-globin proteins. A mutation in either gene could result in a structural hemoglobinopathy. It has only recently become possible to assign an alpha-chain mutant to one of these tw...

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Vydáno v:	J Clin Invest
Hlavní autoři:	Liebhaber, S A, Cash, F E
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	American Society for Clinical Investigation 1985
Témata:	Research Article
On-line přístup:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC423400/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2981252/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI111698
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