Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era

The genetic basis for combined pituitary hormone deficiency (CPHD) is complex, involving 30 genes in a variety of syndromic and nonsyndromic presentations. Molecular diagnosis of this disorder is valuable for predicting disease progression, avoiding unnecessary surgery, and family planning. We expec...

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Pubblicato in:Endocr Rev
Autori principali: Fang, Qing, George, Akima S., Brinkmeier, Michelle L., Mortensen, Amanda H., Gergics, Peter, Cheung, Leonard Y. M., Daly, Alexandre Z., Ajmal, Adnan, Pérez Millán, María Ines, Ozel, A. Bilge, Kitzman, Jacob O., Mills, Ryan E., Li, Jun Z., Camper, Sally A.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Endocrine Society 2016
Soggetti:
Reviews
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5155665/
https://ncbi.nlm.nih.gov/pubmed/27828722
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/er.2016-1101
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