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

Hemoglobin · Published 2026-08-03 · DOI 10.1080/03630269.2026.2676643

Authors (8)

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

Abstract

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Publication details

Year

2026

Citation

Luo, H., Ren, Z., Ye, Y., et al. (2026). Compound Heterozygosity for Hb Port Phillip and the –α 3.7 Deletion Leads to Persistent Hypoxemia in a Chinese Pediatric Family. Hemoglobin. https://doi.org/10.1080/03630269.2026.2676643

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