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

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 endo...

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Detalles Bibliográficos
Autores principales: Luo, Hong-Cheng, Luo, Qi-Sheng, Huang, Fu-Gao, Wang, Chun-Fang, Wei, Ye-Sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5462763/
https://www.ncbi.nlm.nih.gov/pubmed/28592815
http://dx.doi.org/10.1038/s41598-017-03029-9

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