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http://purl.uniprot.org/citations/18628514http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/18628514http://www.w3.org/2000/01/rdf-schema#comment"

Context

Germline mutations in AIP have been recently shown to cause pituitary adenoma predisposition (PAP). Subsequently, many intragenic germline mutations have been reported, both in familial and in sporadic settings.

Objective

Our objective was to evaluate the possible contribution of large genomic germline AIP deletions, an important mutation type in tumor predisposition syndromes, in PAP.

Design

Here, we applied the multiplex ligation-dependent probe amplification assay to examine whether large genomic AIP or MEN1 alterations account for a subset of PAP cases.

Patients

The study was performed on familial and sporadic pituitary adenoma cases of European origin, which had previously tested negative for germline AIP and MEN1 mutations by sequencing.

Results

Two of 21 pituitary adenoma families (9.5%) were found to harbor an AIP deletion. No copy number changes were detected among 67 sporadic pituitary adenoma patients. No MEN1 deletions were found.

Conclusions

The present study shows that large genomic AIP deletions account for a subset of PAP. Therefore, in suspected PAP cases undergoing counseling and AIP genetic testing, multiplex ligation-dependent probe amplification could be considered if direct sequencing does not identify a mutation."xsd:string
http://purl.uniprot.org/citations/18628514http://purl.org/dc/terms/identifier"doi:10.1210/jc.2008-1003"xsd:string
http://purl.uniprot.org/citations/18628514http://purl.uniprot.org/core/author"Paschke R."xsd:string
http://purl.uniprot.org/citations/18628514http://purl.uniprot.org/core/author"Tischkowitz M."xsd:string
http://purl.uniprot.org/citations/18628514http://purl.uniprot.org/core/author"Aaltonen L.A."xsd:string
http://purl.uniprot.org/citations/18628514http://purl.uniprot.org/core/author"Cannavo S."xsd:string
http://purl.uniprot.org/citations/18628514http://purl.uniprot.org/core/author"De Menis E."xsd:string
http://purl.uniprot.org/citations/18628514http://purl.uniprot.org/core/author"Georgitsi M."xsd:string
http://purl.uniprot.org/citations/18628514http://purl.uniprot.org/core/author"Gundogdu S."xsd:string
http://purl.uniprot.org/citations/18628514http://purl.uniprot.org/core/author"Karhu A."xsd:string
http://purl.uniprot.org/citations/18628514http://purl.uniprot.org/core/author"Sane T."xsd:string
http://purl.uniprot.org/citations/18628514http://purl.uniprot.org/core/author"Vierimaa O."xsd:string
http://purl.uniprot.org/citations/18628514http://purl.uniprot.org/core/author"Hodgson S."xsd:string
http://purl.uniprot.org/citations/18628514http://purl.uniprot.org/core/author"Kumar A.V."xsd:string
http://purl.uniprot.org/citations/18628514http://purl.uniprot.org/core/author"Koch C.A."xsd:string
http://purl.uniprot.org/citations/18628514http://purl.uniprot.org/core/author"Izatt L."xsd:string
http://purl.uniprot.org/citations/18628514http://purl.uniprot.org/core/author"Lucassen A."xsd:string
http://purl.uniprot.org/citations/18628514http://purl.uniprot.org/core/author"Salmela P."xsd:string
http://purl.uniprot.org/citations/18628514http://purl.uniprot.org/core/author"Aylwin S."xsd:string
http://purl.uniprot.org/citations/18628514http://purl.uniprot.org/core/author"Bano G."xsd:string
http://purl.uniprot.org/citations/18628514http://purl.uniprot.org/core/author"Heliovaara E."xsd:string
http://purl.uniprot.org/citations/18628514http://purl.uniprot.org/core/date"2008"xsd:gYear
http://purl.uniprot.org/citations/18628514http://purl.uniprot.org/core/name"J Clin Endocrinol Metab"xsd:string
http://purl.uniprot.org/citations/18628514http://purl.uniprot.org/core/pages"4146-4151"xsd:string
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