Work

Compound Heterozygosity for Hb Port Phillip and the –α 3.7 Deletion Leads to Persistent Hypoxemia in a Chinese Pediatric Family

Year: 2026

Type: article

Study design: Case Report

Source: Hemoglobin

DOI: 10.1080/03630269.2026.2676643

Authors: Hualei Luo, Zhenmin Ren, Yuhua Ye, Tao Wu, Xiaoying Fu, Nan Cheng, Jiehua Chen, Yunsheng Chen

Institutions: Shenzhen Children's Hospital, Southern Medical University

Language: English

Topic: Hemoglobinopathies and Related Disorders

Subfield: Genetics

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W7172273294

FWCI:

Cites: 20

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