[Fanconi anemia caused by new compound heterozygous mutation of FANCA gene]

Zhonghua Xue Ye Xue Za Zhi. 2020 Nov 14;41(11):955. doi: 10.3760/cma.j.issn.0253-2727.2020.11.015.

[Article in Chinese]

Authors

J H Sun¹, X J Huang¹, X H Zhang¹, J Z Wang¹, L P Xu¹

Affiliation

¹ Peking University People's Hospital, Peking University Institute of Hematology, National Clinical Research Center for Hematologic Disease, Beijing 100044, China.

PMID: 33333703
PMCID: PMC7767817
DOI: 10.3760/cma.j.issn.0253-2727.2020.11.015

No abstract available

MeSH terms

Fanconi Anemia Complementation Group A Protein* / genetics
Fanconi Anemia* / genetics
Humans
Mutation

Substances

FANCA protein, human
Fanconi Anemia Complementation Group A Protein

Grants and funding

基金项目：国家重点研发计划（2017YFA0104500）