Work

The solute carrier family 26 member 9 modifies rapidly progressing cystic fibrosis associated with homozygous F508del CFTR mutation

Year: 2024

Type: article

Study design: Observational Study

Source: Clinica Chimica Acta

DOI: 10.1016/j.cca.2024.119765

Authors: Shiyu Luo, Stuart Rollins, Klaus Schmitz-Abe, Amy Tam, Qifei Li, Jiahai Shi, Jasmine Lin, Ruobing Wang, Pankaj B. Agrawal

Institutions: Boston Children's Hospital, Harvard University, University of Miami, Jackson Health System, University of Miami Health System, Manton Center for Orphan Disease Research, National University of Singapore, Boston University, Boston Medical Center

Language: English

Topic: Cystic Fibrosis Research Advances

Subfield: Pulmonary and Respiratory Medicine

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: National Institutes of Health, National Heart, Lung, and Blood Institute, National Institute of Mental Health, National Institute on Drug Abuse, National Human Genome Research Institute, National Cancer Institute, National Institute of Neurological Disorders and Stroke

Award: G6455878243

OpenAlex ID: W4399423784

FWCI: 0.866

Cites: 57

Cited by: 3

Related to: 10