Alpha globin gene alterations modifying the phenotype of homozygous beta thalassaemia

Abstract The phenotype of β‐thalassemia varies widely. The primary determinant is the type of beta‐globin gene mutation; however, there are secondary and tertiary modifiers also as associated alpha mutations, polymorphisms, as well as coinheritance of mutations affecting other related systems. Co‐in...

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發表在:	eJHaem
Main Authors:	Jyoti Shaw, Abhilipsa Patra, Anjumana Khatun, Rudra Ray, Amit Ghosh, Sonali Mahapatra, Ashutosh Panigrahi, Maitreyee Bhattacharyya
格式:	Article
語言:	英语
出版:	Wiley 2024-06-01
主題:	alpha deletion alpha‐triplication beta‐thalassemia co‐inheritance homozygous
在線閱讀:	https://doi.org/10.1002/jha2.923