Association of somatotrophinomas with loss of alleles on chromosome 11 and with gsp mutations.

The molecular pathology of somatotrophinomas has been investigated by a combined search for dominant mutations of the gene encoding the Gs alpha protein and for recessive mutations involving chromosome 11q13, which contains the gene causing multiple endocrine neoplasia type 1 (MEN1). Somatotrophinom...

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Bibliographic Details
Main Authors: Thakker, R, Pook, M, Wooding, C, Boscaro, M, Scanarini, M, Clayton, R
Format: Journal article
Language:English
Published: 1993