Outcome of Clinical Genetic Testing in Patients with Features Suggestive for Hereditary Predisposition to PTH-Mediated Hypercalcemia

Primary hyperparathyroidism (pHPT) is associated with familial syndromes such as multiple endocrine neoplasia type 1 (MEN1), 2A (MEN2A), MEN-like syndromes (CDKN1B), and CDC73-related disorder (hyperparathyroidism – jaw tumor syndrome (HPJT)). Familial hypocalciuric hypercalcemia (FHH) caused by CAS...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Horm Cancer
Autors principals: Khairi, Shafaq, Osborne, Jenae, Jacobs, Michelle F, Clines, Gregory T, Miller, Barbra S, Hughes, David T, Else, Tobias
Format: Artigo
Idioma:Inglês
Publicat: Springer US 2020
Matèries:
Original Paper
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7945006/
https://ncbi.nlm.nih.gov/pubmed/32761341
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12672-020-00394-2
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars