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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...
Autores principales: | Sriphrapradang, Chutintorn, Choopun, Kitjapong, Tunteeratum, Atchara, Sura, Thanyachai |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2017
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Materias: | |
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 |
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