Multiple endocrine neoplasia type 1 (MEN1): analysis of 1336 mutations reported in the first decade following identification of the gene.
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterized by the occurrence of tumors of the parathyroids, pancreas, and anterior pituitary. The MEN1 gene, which was identified in 1997, consists of 10 exons that encode a 610-amino acid protein referred to as menin. M...
मुख्य लेखकों: | Lemos, M, Thakker, R |
---|---|
स्वरूप: | Journal article |
भाषा: | English |
प्रकाशित: |
2008
|
समान संसाधन
-
A novel MEN1 intronic mutation associated with multiple endocrine neoplasia type 1.
द्वारा: Lemos, M, और अन्य
प्रकाशित: (2007) -
Multiple endocrine neoplasia type 1 (MEN1).
द्वारा: Thakker, R
प्रकाशित: (2010) -
Multiple endocrine neoplasia type 1 (MEN1).
द्वारा: Pang, J, और अन्य
प्रकाशित: (1994) -
Multiple endocrine neoplasia type 1.
द्वारा: Thakker, R
प्रकाशित: (2000) -
Multiple endocrine neoplasia type 1
द्वारा: Thakker, R
प्रकाशित: (1990)