A novel FLCN mutation in family members diagnosed with primary spontaneous pneumothorax-Reference-Cited by-同舟云学术

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A novel FLCN mutation in family members diagnosed with primary spontaneous pneumothorax

Published:2019-10-18 Issue:12 Volume:7 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Genc Yavuz Burcu¹^ORCID,Guzel Tanoglu Esra²^ORCID,Salman Yılmaz Seda³,Colak Sahin⁴^ORCID

Affiliation:

1. Department of Emergency Medicine University of Health Sciences Fatih Sultan Mehmet Training and Research Center Istanbul Turkey

2. Department of Molecular Biology and Genetics University of Health Sciences Institute of Health Sciences Istanbul Turkey

3. Department of Medical Genetics Cerrahpasa Medical School Istanbul University Istanbul Turkey

4. Department of Emergency Medicine University of Health Sciences Haydarpasa Numune Training and Research Center Istanbul Turkey

Funder

University of Health Sciences

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1003

Reference25 articles.

1. On the inheritance of primary spontaneous pneumothorax

2. Familial spontaneous pneumothorax

3. Familial spontaneous pneumothorax

4. Familial spontaneous pneumothorax in neonates

5. Novel mutations in the folliculin gene associated with spontaneous pneumothorax

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A systematic review assessing the existence of pneumothorax-only variants of FLCN. Implications for lifelong surveillance of renal tumours;European Journal of Human Genetics;2021-07-15

2. Birt–Hogg–Dubé Syndrome: A Rare Genetic Cause of Recurrent Pneumothoraxes in a Young Woman Treated with VATS Pleurectomy—Case Report and Review of the Literature;SN Comprehensive Clinical Medicine;2021-05-07

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