Hemoglobin Wayne: a frameshift mutation detected in human hemoglobin alpha chains.

Hemoglobin Wayne is an alpha chain variant which manifests itself as two minor hemoglobin (Hb) components that migrate more rapidly than Hb A on electrophoresis at pH 8.6. It has been found in a child with Fanconi's anemia and in three generations of the child's family. Each of the minor components...

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Cyhoeddwyd yn:	Proc Natl Acad Sci U S A
Prif Awduron:	Seid-Akhavan, M, Winter, W P, Abramson, R K, Rucknagel, D L
Fformat:	Artigo
Iaith:	Inglês
Cyhoeddwyd:	National Academy of Sciences 1976
Pynciau:	Research Article
Mynediad Ar-lein:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC336023/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1062801/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.73.3.882
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