[A family with hereditary FⅪ deficiency caused by compound heterozygous mutation]

Zhonghua Xue Ye Xue Za Zhi. 2021 Aug 14;42(8):687-689. doi: 10.3760/cma.j.issn.0253-2727.2021.08.014.

[Article in Chinese]

Authors

X Y Zheng¹, Y H Jin¹, Y Y Xu¹, L L Yang¹, L Q Zhu¹, H H Wang¹, S T Jiang¹, M S Wang¹

Affiliation

¹ The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325015, China.

PMID: 34547878
PMCID: PMC8501282
DOI: 10.3760/cma.j.issn.0253-2727.2021.08.014

No abstract available

MeSH terms

Heterozygote
Humans
Mutation*
Pedigree

Grants and funding

基金项目：温州市科技局项目（Y2020110）