Cargando…
A Case of Hyaline Fibromatosis Syndrome with a New Variant of Genetic Mutation in ANTXR2 Gene
Autores principales: | Park, Chan Seong, Lee, Jongeun, Byun, Hyun Jeong, Lim, Youngkyoung, Park, Ji-Hye, Lee, Jong Hee, Lee, Dong-Youn, Lee, Joo-Heung, Yang, Jun-Mo, Lee, Jee Hun, Yoo, So-Young |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Dermatological Association; The Korean Society for Investigative Dermatology
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7997064/ https://www.ncbi.nlm.nih.gov/pubmed/33911680 http://dx.doi.org/10.5021/ad.2019.31.S.S12 |
Ejemplares similares
-
Chronic Exfoliative Cheilitis Successfully Treated by Pinhole Method Using CO(2) Laser
por: Park, Chan Seong, et al.
Publicado: (2019) -
Multiple Scalp Tumors in Juvenile Hyaline Fibromatosis with Antxr-2 Mutation in a Family
por: Mendiratta, Vibhu, et al.
Publicado: (2021) -
Juvenile Hyaline Fibromatosis: Report of a Case with a Novel ANTXR2 Gene Mutation
por: Choochuen, Pongsakorn, et al.
Publicado: (2022) -
CMG2/ANTXR2 regulates extracellular collagen VI which accumulates in hyaline fibromatosis syndrome
por: Bürgi, Jérôme, et al.
Publicado: (2017) -
Juvenile Hyaline Fibromatosis
por: Park, Kyung Tae, et al.
Publicado: (2010)