Co-occurrence of oculocutaneous albinism type 2 and mild sickle cell disease explained by HbS/βthal genotype in an individual from the Democratic Republic of Congo
眼白化病
白化病
色素减退
复合杂合度
遗传学
基因型
生物
移码突变
表型
基因
作者
R Aquaron,Eulalie Lasseaux,Joseph K. Kelekele,Nathalie Bonello‐Palot,Catherine Badens,Benoı̂t Arveiler,Léon Tshilolo