MEN1 935-1GC splicing mutation in an Indian patient with multiple endocrine neoplasia type 1

Background and Objective: Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant syndrome characterized mainly by multiple tumors involving parathyroid, pancreatic, and pituitary glands. To date, there have been no genetic studies reported on MEN1 in the Indian population. In order to b...

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Veröffentlicht in:	Molecular diagnosis & therapy 2007-03, Vol.11 (2), p.129
Hauptverfasser:	Raghavan, Rani, Shah, Sudeep, Kondkar, Altaf A, Dherai, Alpa J, Desai, Devendra, Chauhan, Phulrenu, Lala, Murad, Ashavaid, Tester F
Format:	Artikel
Sprache:	eng
Online-Zugang:	Volltext
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