Open AccessClinical Testing for Mutations in theMEN1Gene in Sweden: A Report on 200 Unrelated Cases
Author(s) -
Emma Tham,
Ulla Grandell,
Eva Lindgren,
Göran Toss,
Britt Skogseid,
Magnus Nordenskjöld
Publication year - 2007
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jc.2007-0476
Subject(s) - men1 , multiple endocrine neoplasia , multiplex ligation dependent probe amplification , mutation , germline mutation , gene mutation , genetics , biology , point mutation , medicine , oncology , cancer research , gene , exon
Multiple endocrine neoplasia type 1 (MEN1) is a tumor syndrome of the parathyroid, endocrine pancreas, and anterior pituitary caused by mutations in the MEN1 gene on 11q13.
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