Clinical Features and Mutations in the ENG, ACVRL1, and SMAD4 genes in Korean Patients with Hereditary Hemorrhagic Telangiectasia

Hereditary hemorrhagic telangiectasia (HHT) is an inherited disorder that is characterized by abnormal communication between the arteries and veins in the skin, mucosa, and various organs. HHT has been reported to show significant phenotypic variability and genetic heterogeneity with wide ethnic and...

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Detalles Bibliográficos
Autores principales: Lee, Seung-Tae, Kim, Jee-Ah, Jang, Shin-Yi, Kim, Duk-Kyung, Do, Young Soo, Suh, Gee Young, Kim, Jong-Won, Ki, Chang-Seok
Formato: Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2009
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2650970/
https://www.ncbi.nlm.nih.gov/pubmed/19270816
http://dx.doi.org/10.3346/jkms.2009.24.1.69

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2650970/
https://www.ncbi.nlm.nih.gov/pubmed/19270816
http://dx.doi.org/10.3346/jkms.2009.24.1.69

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