Bibliometric Analysis of Birt-Hogg-Dubé Syndrome From 2001 to 2021

Bibliometric Analysis of Birt-Hogg-Dubé Syndrome From 2001 to 2021

BackgroundBirt-Hogg-Dubé syndrome (BHD) is a rare autosomal dominant inherited disorder caused by germline mutations in folliculin (FLCN). Despite our significantly evolved understanding of BHD over the past decades, no bibliometric analyses have been conducted in this field. This study aimed to ana...

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Bibliographic Details
Main Authors: Shixu Liu, Kun Xia, Xiaohong Liu, Yuanyuan Duan, Mu Hu, Hongsheng Xia, Jiayu Lv, Lili Zhang, Yanyi Liu, Xiao Xia, Guangxi Li, Xiangning Cui
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-04-01
Series:Frontiers in Medicine
Subjects:
Birt-Hogg-Dubé syndrome (BHD)
FLCN
folliculin
bibliometric analysis
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Online Access:https://www.frontiersin.org/articles/10.3389/fmed.2022.857127/full

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https://www.frontiersin.org/articles/10.3389/fmed.2022.857127/full

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