Novel Glial Cells Missing-2 (GCM2) variants in parathyroid disorders

OBJECTIVE: The aim of this study was to analyze variants of the gene glial cells missing-2 (GCM2), encoding a parathyroid cell-specific transcription factor, in familial hypoparathyroidism and in familial isolated hyperparathyroidism (FIHP) without and with parathyroid carcinoma. DESIGN: We characte...

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Detalles Bibliográficos
Autores principales: Canaff, Lucie, Guarnieri, Vito, Kim, Yoojung, Wong, Betty Y L, Nolin-Lapalme, Alexis, Cole, David E C, Minisola, Salvatore, Eller-Vainicher, Cristina, Cetani, Filomena, Repaci, Andrea, Turchetti, Daniela, Corbetta, Sabrina, Scillitani, Alfredo, Goltzman, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2022
Materias:
Clinical Study
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8859918/
https://www.ncbi.nlm.nih.gov/pubmed/35038313
http://dx.doi.org/10.1530/EJE-21-0433

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8859918/
https://www.ncbi.nlm.nih.gov/pubmed/35038313
http://dx.doi.org/10.1530/EJE-21-0433

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