Cargando…
Pathogenic effect of a TGFBR1 mutation in a family with Loeys–Dietz syndrome
BACKGROUND: Thoracic aortic aneurysms and dissections (TAAD) may have a heritable cause in up to 20% of cases. We aimed to investigate the pathogenic effect of a TGFBR1 mutation in relation to TAAD. METHODS: Co‐segregation analysis was performed followed by functional investigations, including myoge...
Autores principales: | Cozijnsen, Luc, Plomp, Astrid S., Post, Jan G., Pals, Gerard, Bogunovic, Natalija, Yeung, Kak K., Niessen, Hans W. M., Goumans, Marie‐José T. H., Barge‐Schaapveld, Daniela Q. C. M., Micha, Dimitra |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6785444/ https://www.ncbi.nlm.nih.gov/pubmed/31475485 http://dx.doi.org/10.1002/mgg3.943 |
Ejemplares similares
-
Identification of a Pathogenic TGFBR2 Variant in a Patient With Loeys–Dietz Syndrome
por: Luo, Xi, et al.
Publicado: (2020) -
Surgical Outcome and Histological Differences between Individuals with TGFBR1 and TGFBR2 Mutations in Loeys-Dietz Syndrome
por: Seike, Yoshimasa, et al.
Publicado: (2021) -
Novel Pathogenic Variant in TGFBR2 Confirmed by Molecular Modeling Is a Rare Cause of Loeys-Dietz Syndrome
por: Zimmermann, Michael T., et al.
Publicado: (2017) -
TGFBR3 variation is not a common cause of Marfan-like syndrome and Loeys-Dietz-like syndrome
por: Singh, Krishna K, et al.
Publicado: (2012) -
Valve-sparing aortic root replacement in Loeys-Dietz syndrome and a novel mutation in TGFBR2
por: Kasar, Taner, et al.
Publicado: (2018)