Primary Spontaneous Pneumothorax
Last Posted: Aug 02, 2021
- Association of Alpha 1-antitrypsin Deficiency and Genetic Predisposition in Primary Spontaneous Pneumothorax.
Sahin Taner, et al. Journal of the College of Physicians and Surgeons--Pakistan : JCPSP 2021 7 (7) 775-779
- A rapid NGS strategy for comprehensive molecular diagnosis of Birt-Hogg-Dubé syndrome in patients with primary spontaneous pneumothorax.
Zhang Xinxin et al. Respiratory research 2016 May 17(1) 64
- Multicentric Genome-Wide Association Study for Primary Spontaneous Pneumothorax.
Sousa Inês, et al. PloS one 2016 0 (5) e0156103
- FLCN intragenic deletions in Chinese familial primary spontaneous pneumothorax.
Ding Yibing, et al. American journal of medical genetics. Part A 2015 5 (5) 1125-33
- Primary spontaneous pneumothorax
From NCATS Genetic and Rare Diseases Information Center
- Mutation analysis of the FLCN gene in Chinese patients with sporadic and familial isolated primary spontaneous pneumothorax.
Ren H-Z, et al. Clinical genetics 2008 8 (2) 178-83
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Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
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