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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...

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Main Authors: Salvatori, Roberto, Daly, Adrian F, Quinones-Hinojosa, Alfredo, Thiry, Albert, Beckers, Albert
格式: Artigo
語言:Inglês
出版: Bioscientifica Ltd 2014
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在線閱讀: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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