TNFRSF13B c.226G>A (p.Gly76Ser) as a Novel Causative Mutation for Pulmonary Arterial Hypertension

BACKGROUND: Recently, some studies reported the pulmonary artery hypertension (PAH)–associated genes. However, a majority of patients with familial or sporadic PAH lack variants in the known pathogenic genes. In this study, we investigated the new causative gene variants associated with PAH. METHODS...

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Detalles Bibliográficos
Autores principales: Shinya, Yoshiki, Hiraide, Takahiro, Momoi, Mizuki, Goto, Shinichi, Suzuki, Hisato, Katsumata, Yoshinori, Kurebayashi, Yutaka, Endo, Jin, Sano, Motoaki, Fukuda, Keiichi, Kosaki, Kenjiro, Kataoka, Masaharu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Brief Communications
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8174299/
https://www.ncbi.nlm.nih.gov/pubmed/33586470
http://dx.doi.org/10.1161/JAHA.120.019245

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