Frequent occurrence of an intron 4 mutation in multiple endocrine neoplasia type 1.

MEN1 is an autosomal dominant disorder characterized by parathyroid, pituitary, and pancreatic tumors. The MEN1 gene is located on chromosome 11q13 and encodes a 610-amino acid protein. MEN1 mutations are of diverse types and are scattered throughout the coding region, such that almost every MEN1 fa...

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Bibliographic Details
Main Authors:	Turner, J, Leotlela, P, Pannett, A, Forbes, SA, Bassett, J, Harding, B, Christie, P, Bowen-Jones, D, Ellard, S, Hattersley, A, Jackson, C, Pope, R, Quarrell, O, Trembath, R, Thakker, R
Format:	Journal article
Language:	English
Published:	2002

Frequent occurrence of an intron 4 mutation in multiple endocrine neoplasia type 1.

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