Diffuse Panbronchiolitis
What's New
Last Posted: Mar 04, 2023
- Primary ciliary dyskinesia caused by a large homozygous deletion including exons 1-4 of DRC1 in Japanese patients with recurrent sinopulmonary infection.
Keicho Naoto, et al. Molecular genetics & genomic medicine 2019 0 (1) e1033 - Recurring large deletion in DRC1 (CCDC164) identified as causing primary ciliary dyskinesia in two Asian patients.
Morimoto Kozo, et al. Molecular genetics & genomic medicine 2019 0 (8) e838 - Effect of diffuse panbronchiolitis critical region 1 polymorphisms on the risk of aspirin-exacerbated respiratory disease in Korean asthmatics.
Lee Jin Sol, et al. Respiratory care 2012 5 (5) 758-63 - Diffuse panbronchiolitis
From NCATS Genetic and Rare Diseases Information Center - [Human leukocyte antigen genes to genetic predisposition in diffuse panbronchiolitis].
Shen Ce, et al. Zhonghua jie he he hu xi za zhi = Zhonghua jiehe he huxi zazhi = Chinese journal of tuberculosis and respiratory diseases 2008 4 (4) 272-6 - Mannose-binding lectin gene polymorphism is a modulating factor in repeated respiratory infections.
Gomi Kazunori, et al. Chest 2004 7 (1) 95-9 - [Genetic variation of NADPH/NADH oxidase and susceptibility to diffuse panbronchiolitis (DPB) and chronic obstructive pulmonary disease (COPD)].
Ishii T, et al. Nihon Koky?ki Gakkai zasshi = the journal of the Japanese Respiratory Society 2001 5 (5) 328-32
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Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
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- Page last reviewed:Feb 1, 2024
- Page last updated:May 18, 2024
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