α-thalassaemia combined with hereditary spherocytosis in the same patient

A family of four from the Guangxi Zhuang Autonomous Region of China, including a child with α-thalassaemia and hereditary spherocytosis (HS), underwent laboratory identification, and genetic analysis. After harvesting peripheral blood samples from the child patient and his family members, GAP-polyme...

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Detalles Bibliográficos
Autores principales: Li, Xiaohong, Liao, Lin, Deng, Xuelian, Huang, Jian, Deng, Zengfu, Wei, Hongying, Mo, Wuning, Lin, Faquan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5774485/
https://www.ncbi.nlm.nih.gov/pubmed/29434716
http://dx.doi.org/10.3892/etm.2017.5579

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5774485/
https://www.ncbi.nlm.nih.gov/pubmed/29434716
http://dx.doi.org/10.3892/etm.2017.5579

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