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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: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Bioscientifica Ltd
2014
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| Assuntos: | |
| Acceso en liña: | 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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