Código QR

The rare hemoglobin variants Hb O-Arab and Hb D-Punjab identified in population-based genetic screening throughout Guangxi, China

BackgroundHemoglobinopathies are a group of autosomal recessive disorders characterized by a high degree of clinical and genetic heterogeneity. Comprehensive genetic screening for hemoglobin variants is crucial for prevention and treatment of these conditions. Single-molecule real-time (SMRT) sequen...

Descrición completa

Gardado en:
Detalles Bibliográficos
Principais autores: Chunrong Gui, Zifeng Cheng, Yongsheng Chen, Yunting Ma, Hongfei Chen, Wei Wei, Xianda Wei, Juliang Liu, Xu Zhou, Qianqian Du, Yinghui Lai, Baoheng Gui
Formato: Artigo
Idioma:Inglês
Publicado: Frontiers Media S.A. 2025-08-01
Series:Frontiers in Genetics
Assuntos:
Acceso en liña:https://www.frontiersin.org/articles/10.3389/fgene.2025.1622391/full
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!