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Article

Impact of genotype on endocrinal complications of Children with Alpha-thalassemia in China.

Scientific reports - 7 Jun 2017

Luo Hong-Cheng, Luo Qi-Sheng, Huang Fu-Gao, Wang Chun-Fang, Wei Ye-Sheng

Abstract excerpt

Alpha-thalassemia occurs with high frenquency in China. Four common α-globin gene deletion mutations (-SEA, -α3.7, and -α4.2, Haemoglobin Constant Spring (CS) mutation) were identified in Chinese patients. Individuals with alpha-thalassemia syndrome are more often of children. However report on endocrinal complications in children with alpha thalassemia in China are still absent. The present study aimed to...

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Identifiers

PMID: 28592815
DOI: 10.1038/s41598-017-03029-9
PMCID: PMC5462763

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SEA

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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