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

BACKGROUND: Birt-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 a...

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Detalles Bibliográficos
Autores principales: Liu, Shixu, Xia, Kun, Liu, Xiaohong, Duan, Yuanyuan, Hu, Mu, Xia, Hongsheng, Lv, Jiayu, Zhang, Lili, Liu, Yanyi, Xia, Xiao, Li, Guangxi, Cui, Xiangning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9035795/
https://www.ncbi.nlm.nih.gov/pubmed/35479937
http://dx.doi.org/10.3389/fmed.2022.857127

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9035795/
https://www.ncbi.nlm.nih.gov/pubmed/35479937
http://dx.doi.org/10.3389/fmed.2022.857127

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