alpha-Thalassemia caused by an unstable alpha-globin mutant.

In a previous study, molecular cloning of the alpha-globin genes from a patient with nondeletion Hb-H disease (genotype--/alpha alpha) showed that a single nucleotide mutation (CTG to CCG) in one of the genes resulted in a leucine to proline substitution. This paper describes the approach we used to...

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Argitaratua izan da:	J Clin Invest
Egile Nagusiak:	Liebhaber, S A, Kan, Y W
Formatua:	Artigo
Hizkuntza:	Inglês
Argitaratua:	American Society for Clinical Investigation 1983
Gaiak:	Research Article
Sarrera elektronikoa:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC436893/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6826718/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI110790
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