GPR101 Mutations are not a frequent cause of Congenital Isolated Growth Hormone Deficiency

OBJECTIVE: Patients with Xq26.3 microduplication present early-childhood gigantism due to marked growth hormone (GH) hypersecretion from mixed GH-PRL adenomas and hyperplasia. The microduplication includes GPR101 which is upregulated in patients’ tumor tissue. The GPR101 gene codes for an orphan G p...

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Detalhes bibliográficos
Publicado no:Horm Metab Res
Main Authors: Castinetti, Frederic, Daly, Adrian F., Stratakis, Constantine A., Caberg, Jean-Hubert, Castermans, Emilie, Trivellin, Giampaolo, Rostomyan, Liliya, Saveanu, Alexandru, Jullien, Nicolas, Reynaud, Rachel, Barlier, Anne, Bours, Vincent, Brue, Thierry, Beckers, Albert
Formato: Artigo
Idioma:Inglês
Publicado em: 2016
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7566854/
https://ncbi.nlm.nih.gov/pubmed/26797872
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0042-100733
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