Compounded with hemoglobin Port Phillip and ‐α(4.2) or ‐‐(SEA) deletions were identified in Chinese population

INTRODUCTION: Although over 1000 hemoglobin (Hb) variants were identified so far, Hb Port Phillip compound with α‐thalassemia deletion had no reported before. METHODS: Two patients and the associated families from Guangdong province in China were recruited. Hematological parameters were determined b...

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Detalles Bibliográficos
Autores principales: Du, Li, Bao, Xiuqin, Qin, Danqing, Wang, Jicheng, Yao, Cuize, Liang, Jie, Chen, Jianhong, Yin, Aihua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Clinical Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8457688/
https://www.ncbi.nlm.nih.gov/pubmed/34398528
http://dx.doi.org/10.1002/mgg3.1699

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8457688/
https://www.ncbi.nlm.nih.gov/pubmed/34398528
http://dx.doi.org/10.1002/mgg3.1699

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