Mutations in proteasome-related genes are associated with thyroid hemiagenesis

PURPOSE: Human thyroid development is a complex and still unexplained process. Thyroid hemiagenesis is a congenital anomaly, where one of the thyroid lobes fails to develop. In the majority of patients with thyroid hemiagenesis, the genetic background remains unknown. The aim of the study was to sea...

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Detalhes bibliográficos
Publicado no:Endocrine
Main Authors: Budny, Bartlomiej, Szczepanek-Parulska, Ewelina, Zemojtel, Tomasz, Szaflarski, Witold, Rydzanicz, Malgorzata, Wesoly, Joanna, Handschuh, Luiza, Wolinski, Kosma, Piatek, Katarzyna, Niedziela, Marek, Ziemnicka, Katarzyna, Figlerowicz, Marek, Zabel, Maciej, Ruchala, Marek
Formato: Artigo
Idioma:Inglês
Publicado em: Springer US 2017
Assuntos:
Endocrine Genetics/Epigenetics
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5395596/
https://ncbi.nlm.nih.gov/pubmed/28390009
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12020-017-1287-4
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