A novel MEN1 intronic mutation associated with multiple endocrine neoplasia type 1.

A novel MEN1 intronic mutation associated with multiple endocrine neoplasia type 1.

OBJECTIVE: To investigate a family with an unusual combination of multiple endocrine neoplasia (MEN1) and the McCune-Albright syndrome for MEN1 mutations and activating GNAS1 mutations at codons Arg201 and Gln227. METHODS: DNA sequences analyses were performed of the MEN1 gene and codons Arg201 and...

Disgrifiad llawn

Manylion Llyfryddiaeth
Prif Awduron:	Lemos, M, Harding, B, Shalet, S, Thakker, R
Fformat:	Journal article
Iaith:	English
Cyhoeddwyd:	2007

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