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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2017
Materias:
Endocrine Genetics/Epigenetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5395596/
https://www.ncbi.nlm.nih.gov/pubmed/28390009
http://dx.doi.org/10.1007/s12020-017-1287-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5395596/
https://www.ncbi.nlm.nih.gov/pubmed/28390009
http://dx.doi.org/10.1007/s12020-017-1287-4

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