Hemoglobin Evanston (alpha 14 Trp----Arg). An unstable alpha-chain variant expressed as alpha-thalassemia.

A new hematologic syndrome with phenotypic features of mild Hb H disease was identified in three children from two unrelated black American families. Erythrocytes from each of these children contained Hb H (beta 4) and Hb Barts (gamma 4), as well as a slowly migrating hemoglobin fraction that made u...

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Bibliographische Detailangaben
Hauptverfasser: Honig, G R, Shamsuddin, M, Vida, L N, Mompoint, M, Valcourt, E, Bowie, L J, Jones, E C, Powers, P A, Spritz, R A, Guis, M
Format: Artigo
Sprache:Inglês
Veröffentlicht: 1984
Schlagworte:
Research Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC437086/
https://ncbi.nlm.nih.gov/pubmed/6725558
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