Genetic counseling and prenatal decision for hemoglobin H disease caused by the rare α2 codon 30 (-GAG) (HBA2: c.91_93delGAG) mutation and the SEA deletion: Case series study

Objective: We report a rare mutation on the α2-globin gene, HBA2: c.91_93delGAG and its potential functions. Case Report: We mainly described four patients with hemoglobin (Hb) H disease caused by the rare mutation and the SEA deletion but diversity in clinical presentation. Two had survived to adul...

Full description

Saved in:
Bibliographic Details
Main Authors: Zhi-Yang Guan (Author), Ze-Yan Zhong (Author), Hai-Lin He (Author), Dan Chen (Author), Guo-Xing Zhong (Author), Kun-Xiang Yang (Author), Jian-Hong Chen (Author)
Format: Book
Published: Elsevier, 2021-07-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

Internet

Connect to this object online.

3rd Floor Main Library

Holdings details from 3rd Floor Main Library
Call Number: A1234.567
Copy 1 Available