An atypical pulmonary fibrosis is associated with co-inheritance of mutations in the calcium binding protein genes S100A3 and S100A13 .

Autor: Al-Mutairy EA; Dept of Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.; Dept of Cell Biology, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.; College of Medicine, Al-Faisal University, Riyadh, Saudi Arabia., Imtiaz FA; Dept of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Khalid M; Dept of Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Al Qattan S; Dept of Cell Biology, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Saleh S; Dept of Cell Biology, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Mahmoud LM; BioMolecular Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Al-Saif MM; BioMolecular Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Al-Haj L; BioMolecular Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Al-Enazi A; Dept of Cell Biology, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., AlJebreen AM; Dept of Radiology, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Mohammed SF; Dept of Pathology and Laboratory Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Mobeireek AF; Dept of Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Alkattan K; Dept of Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.; College of Medicine, Al-Faisal University, Riyadh, Saudi Arabia., Chisti MA; Dept of Dermatology, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Luzina IG; University of Maryland School of Medicine, Baltimore, MD, USA.; Baltimore VA Medical Center, Baltimore, MD, USA., Al-Owain M; College of Medicine, Al-Faisal University, Riyadh, Saudi Arabia.; Dept of Medical Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Weheba I; Dept of Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.; National Research Centre, Cairo, Egypt., Abdelsayed AM; Dept of Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.; Ain Shams University, Cairo, Egypt., Ramzan K; Dept of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Janssen LJ; St Joseph's Hospital and Dept of Medicine, McMaster University, Hamilton, ON, Canada., Conca W; Dept of Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.; Dept of Cell Biology, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.; College of Medicine, Al-Faisal University, Riyadh, Saudi Arabia., Alaiya A; Stem Cell Therapy Program, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Collison KS; Dept of Cell Biology, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Meyer BF; Dept of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Atamas SP; University of Maryland School of Medicine, Baltimore, MD, USA.; Baltimore VA Medical Center, Baltimore, MD, USA., Khabar KS; College of Medicine, Al-Faisal University, Riyadh, Saudi Arabia.; BioMolecular Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia., Hasday JD; University of Maryland School of Medicine, Baltimore, MD, USA.; Baltimore VA Medical Center, Baltimore, MD, USA., Al-Mohanna F; Dept of Cell Biology, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia futwan@kfshrc.edu.sa.; College of Medicine, Al-Faisal University, Riyadh, Saudi Arabia.

Publikováno v: The European respiratory journal [Eur Respir J] 2019 Jul 18; Vol. 54 (1). Date of Electronic Publication: 2019 Jul 18 (Print Publication: 2019).