Co-inheritance of G6PD deficiency and 211 G to a variation of UGT1A1 in neonates with hyperbilirubinemia in eastern Guangdong

BACKGROUND: Glucose-6-phosphate dehydrogenase (G6PD) deficiency, which may manifest as neonatal hyperbilirubinemia, is the most prevalent erythrocytic enzyme-related disease in the world. OBJECTIVE: To investigate the association between neonatal hyperbilirubinemia and co-inheritance of G6PD deficie...

Descripción completa

Detalles Bibliográficos
Autores principales: Xu, Jia-Xin, Lin, Fen, Chen, Zi-Kai, Luo, Zhao-Yun, Zhan, Xiao-Fen, Wu, Jiao-Ren, Ma, Yu-Bin, Li, Jian-Dong, Yang, Li-Ye
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8665559/
https://www.ncbi.nlm.nih.gov/pubmed/34895177
http://dx.doi.org/10.1186/s12887-021-03010-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8665559/
https://www.ncbi.nlm.nih.gov/pubmed/34895177
http://dx.doi.org/10.1186/s12887-021-03010-6

Ejemplares similares