ZCCHC8 p.P410A disrupts nucleocytoplasmic localization, promoting idiopathic pulmonary fibrosis and chronic obstructive pulmonary disease
We may first report the ZCCHC8 mutation in Asian population with IPF. Our study broadens the mutation, phenotype, and population spectrum of ZCCHC8 deficiency.
Authors
- Si‐Hua Chang
- Lv Liu (ORCID: https://orcid.org/0000-0001-9719-9930)
- Yi-Qiao Hu
- Liang‐Liang Fan (ORCID: https://orcid.org/0000-0001-7431-1838)
- Chenyu Wang (ORCID: https://orcid.org/0000-0001-7135-7662)
- Hong Luo (ORCID: https://orcid.org/0009-0006-3463-3238)
- Cheng-Feng Hu
Institutions
- Central South University (CN)
- Second Xiangya Hospital of Central South University (CN)
Publication Details
- Journal
- Molecular Medicine
- Published
- 2024-09-10
- DOI
- https://doi.org/10.1186/s10020-024-00913-9
- Citations
- 4
- Primary Topic
- Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
- Type
- article
- Field-Weighted Citation Impact
- 1.68
Funders
- National Natural Science Foundation of China
- Central South University
- Natural Science Foundation of Hunan Province
- Xiangya Hospital, Central South University