Skip to content

1 paper indexed here

We haven’t gathered this author’s papers yet. Follow them and we’ll fetch their work.

Not the right person? Other researchers publish under this name.

Open access Sep 2026

Clinical characteristics, genotype-phenotype correlation, and prognostic follow-up of 48 Chinese children with hereditary spherocytosis

The largest Chinese single-center cohort with the longest reported follow-up of pediatric HS, featuring distinct local mutational profiles enriches the Chinese HS mutation spectrum and guides clinical management, genetic counseling and future gene therapy research for pediatric HS.

Fei Xie, Yu Gao, Lu Gan et al. · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.