FLCNintragenic deletions in Chinese familial primary spontaneous pneumothorax-Reference-Cited by-同舟云学术

FLCNintragenic deletions in Chinese familial primary spontaneous pneumothorax

Published:2015-03-21 Issue:5 Volume:167 Page:1125-1133
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Ding Yibing¹²,Zhu Chengchu³,Zou Wei⁴,Ma Dehua³,Min Haiyan¹²,Chen Baofu³,Ye Minhua³,Pan Yanqing⁴,Cao Lei⁴,Wan Yueming⁴,Zhang Wenwen¹,Meng Lulu¹,Mei Yuna¹,Yang Chi¹,Chen Shilin³,Gao Qian¹²,Yi Long¹²

Affiliation:

1. Center for Translational Medicine; Nanjing University Medical School; Nanjing China

2. Jiangsu Key Laboratory for Molecular Medicine; Nanjing University Medical School; Nanjing China

3. Department of Cardiothoracic Surgery; Taizhou Hospital of Zhejiang Province; Wenzhou Medical University; Linhai China

4. Department of Thoracic Surgery; Nanjing Chest Hospital; Nanjing China

Funder

National Basic Research Program of China

National Natural Science Foundation of China

Science and Technology Project of Jiangsu Province

Ph.D. Programs Foundation of Ministry of Education of China

Jiangsu Province Health Department of Medicine leading talent and innovation team project

Foundation of Nanjing Municipal Public Health Bureau

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference29 articles.

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2. The discovery of a Persian family with a form of Birt-Hogg-Dubé syndrome lacking the typical cutaneous stigmata of the syndrome;Babaei Jandaghi;Clin Imaging,2013

3. Folliculin encoded by the BHD gene interacts with a binding protein FNIP1 and AMPK, and is involved in AMPK and MTOR signalling;Baba;Proc Natl Acad Sci USA,2006

4. Identification of intragenic deletions and duplication in the FLCN gene in Birt-Hogg-Dubé syndrome;Benhammou;Genes Chromosomes Cancer,2011

5. Faster sequential genetic linkage computations;Cottingham;Am J Hum Genet,1993

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