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Erratum to: A new mutation in the menin gene causes the multiple endocrine neoplasia type 1 syndrome with adrenocortical carcinoma

โœ Scribed by M. Haase; M. Anlauf; M. Schott; S. Schinner; E. Kaminsky; W. A. Scherbaum; Holger S. Willenberg


Book ID
107571547
Publisher
Springer
Year
2011
Tongue
English
Weight
91 KB
Volume
39
Category
Article
ISSN
0969-711X

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Lack of allelic loss at the multiple end
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The gene responsible for multiple endocrine neoplasia type I (MEN-l) syndrome has been mapped to chromosome l lq13. It appears to function as a tumoursuppressor gene analogous to that for retinoblastoma and allelic losses involving the wild-type of the MEN-1 allele have been found in parathyroid and