Genotype-Phenotype Correlation in Patients With Germline Mutations of VHL, RET, SDHB, and SDHD Genes: Thai Experience

Mutations in the VHL, RET, SDHB, and SDHD genes are responsible for von Hippel-Lindau (VHL) disease, multiple endocrine neoplasia type 2 (MEN2), and familial paraganglioma, respectively. However, genotype-phenotype correlation data are lacking in Southeast Asia. A retrospective medical chart review...

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Detalles Bibliográficos
Autores principales: Sriphrapradang, Chutintorn, Choopun, Kitjapong, Tunteeratum, Atchara, Sura, Thanyachai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2017
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5404897/
https://www.ncbi.nlm.nih.gov/pubmed/28469506
http://dx.doi.org/10.1177/1179551417705122

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5404897/
https://www.ncbi.nlm.nih.gov/pubmed/28469506
http://dx.doi.org/10.1177/1179551417705122

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