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A clinically novel AIP mutation in a patient with a very large, apparently sporadic somatotrope adenoma
Heterozygous germline inactivating mutations in the aryl hydrocarbon receptor-interacting protein (AIP) gene lead to pituitary adenomas that most frequently present in the setting of familial isolated pituitary adenoma syndrome, usually as somatotropinomas and prolactinomas. More recently, they have...
Gorde:
| Egile Nagusiak: | , , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Bioscientifica Ltd
2014
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4120360/ https://ncbi.nlm.nih.gov/pubmed/25136448 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1530/EDM-14-0048 |
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