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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Detaylı Bibliyografya
Yayımlandı:J Clin Endocrinol Metab
Asıl Yazarlar: Sahasrabudhe, Ruta, Stultz, Jacob, Williamson, John, Lott, Paul, Estrada, Ana, Bohorquez, Mabel, Palles, Claire, Polanco-Echeverry, Guadalupe, Jaeger, Emma, Martin, Lynn, Echeverry, Maria Magdalena, Tomlinson, Ian, Carvajal-Carmona, Luis G.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Endocrine Society 2016
Konular:
Original Articles
Online Erişim: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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