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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Bibliografiska uppgifter
I publikationen:Endocrine
Huvudupphovsmän: 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
Materialtyp: Artigo
Språk:Inglês
Publicerad: Springer US 2017
Ämnen:
Endocrine Genetics/Epigenetics
Länkar: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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