Current and emerging therapies for PNETs in patients with or without MEN1
Pancreatic neuroendocrine tumours (PNETs) might occur as a non-familial isolated endocrinopathy or as part of a complex hereditary syndrome, such as multiple endocrine neoplasia type 1 (MEN1). MEN1 is an autosomal dominant disorder characterized by the combined occurrence of PNETs with tumours of th...
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| Format: | Journal article |
| Published: |
Nature Publishing Group
2018
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