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Clinical and molecular genetic features of Hb H and AE Bart’s diseases in central Thai children

BACKGROUND: α-Thalassemia, one of the major thalassemia types in Thailand, is caused by either deletion or non-deletional mutation of one or both α-globin genes. Inactivation of three α-globin genes causes hemoglobin H (Hb H) disease, and the combination of Hb H disease with heterozygous hemoglobin...

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Bibliografiset tiedot
Julkaisussa:Appl Clin Genet
Päätekijät: Traivaree, Chanchai, Boonyawat, Boonchai, Monsereenusorn, Chalinee, Rujkijyanont, Piya, Photia, Apichat
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Dove Medical Press 2018
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5892615/
https://ncbi.nlm.nih.gov/pubmed/29662324
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/TACG.S161152
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