Work

Mutation analysis of the FLCN gene in Chinese patients with sporadic and familial isolated primary spontaneous pneumothorax

Year: 2008

Type: article

Study design: Observational Study

Source: Clinical Genetics

DOI: 10.1111/j.1399-0004.2008.01030.x

Authors: H‐Z Ren, C‐C Zhu, C Yang, S‐L Chen, J Xie, Y‐Y Hou, Z‐F Xu, D‐J Wang, D‐K Mu, D‐H Ma, Y Wang, M‐H Ye, Z‐R Ye, B‐F Chen, C‐G Wang, J Lin, D Qiao, L Yi

Institutions: Nanjing Drum Tower Hospital, Zhejiang Taizhou Hospital, Nanjing University, Nanjing Maternity and Child Health Care Hospital, Nanjing Medical University

Language: English

Topic: Tuberous Sclerosis Complex Research

Subfield: Genetics (clinical)

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: Brigham Young University

OpenAlex ID: W2160070102

FWCI: 1.888

Cites: 24

Cited by: 83

Related to: 10