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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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Endocrine
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Springer US 2017
Gaiak:
Endocrine Genetics/Epigenetics
Sarrera elektronikoa: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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