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The HABP2 G534E Variant Is an Unlikely Cause of Familial Nonmedullary Thyroid Cancer
CONTEXT: A recent study reported the nonsynonymous G534E (rs7080536, allele A) variant in the HABP2 gene as causal in familial nonmedullary thyroid cancer (NMTC). OBJECTIVE: The objective of this study was to evaluate the causality of HABP2 G534E in the TCUKIN study, a multicenter population-based s...
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| Publicado no: | J Clin Endocrinol Metab |
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| Main Authors: | , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Endocrine Society
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4803181/ https://ncbi.nlm.nih.gov/pubmed/26691890 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2015-3928 |
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