SEMA3A and IGSF10 Are Novel Contributors to Combined Pituitary Hormone Deficiency (CPHD)

Background: The mutation frequencies of pituitary transcription factors genes in patients with combined pituitary hormone deficiencies (CPHD) vary substantially between populations. However, apart from PROP1 the mutation rate of other genes is low and for almost half of the patients with CPHD the ro...

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Pubblicato in:Front Endocrinol (Lausanne)
Autori principali: Budny, Bartlomiej, Zemojtel, Tomasz, Kaluzna, Malgorzata, Gut, Pawel, Niedziela, Marek, Obara-Moszynska, Monika, Rabska-Pietrzak, Barbara, Karmelita-Katulska, Katarzyna, Stajgis, Marek, Ambroziak, Urszula, Bednarczuk, Tomasz, Wrotkowska, Elzbieta, Bukowska-Olech, Ewelina, Jamsheer, Aleksander, Ruchala, Marek, Ziemnicka, Katarzyna
Natura: Artigo
Lingua:Inglês
Pubblicazione: Frontiers Media S.A. 2020
Soggetti:
Endocrinology
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7308526/
https://ncbi.nlm.nih.gov/pubmed/32612575
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fendo.2020.00368
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