Genetic screening methods for the detection of mutations responsible for multiple endocrine neoplasia type 1
✍ Scribed by Katalin Balogh; Attila Patócs; Judit Majnik; Károly Rácz; László Hunyady
- Book ID
- 116987559
- Publisher
- Elsevier Science
- Year
- 2004
- Tongue
- English
- Weight
- 490 KB
- Volume
- 83
- Category
- Article
- ISSN
- 1096-7192
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Multiple endocrine neoplasia type 1 (MEN 1) is a familial cancer syndrome characterized by parathyroid hyperplasia, pituitary adenomas, and neuroendocrine tumors of the pancreas and duodenum. In 1997, the MEN1 tumor suppressor gene was identified, and numerous germline mutations have been reported t
Multiple endocrine neoplasia–type 1 (MEN1) is an autosomal dominant familial cancer syndrome characterized by tumors in parathyroids, enteropancreatic endocrine tissues, and the anterior pituitary. DNA sequencing from a previously identified minimal interval on chromosome 11q13 identified several ca