A novel germline mutation at exon 10 of MEN1 gene: a clinical survey and positive genotype-phenotype analysis of a MEN1 Italian family, including monozygotic twins-Reference-Cited by-同舟云学术

A novel germline mutation at exon 10 of MEN1 gene: a clinical survey and positive genotype-phenotype analysis of a MEN1 Italian family, including monozygotic twins

Published:2018-08-06 Issue:3 Volume:17 Page:427-435
ISSN:1109-3099
Container-title:Hormones
language:en
Short-container-title:Hormones

Author:

Palermo Andrea,Capoluongo Ettore,Del Toro Rossella,Manfrini Silvia,Pozzilli Paolo,Maggi Daria,Defeudis Giuseppe,Pantano Francesco,Coppola Roberto,Di Matteo Francesco Maria,Raffaelli Marco,Concolino Paola,Falchetti Alberto

Publisher

Springer Science and Business Media LLC

Subject

General Medicine,Endocrinology, Diabetes and Metabolism

Link

http://link.springer.com/article/10.1007/s42000-018-0044-2/fulltext.html

Reference37 articles.

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3. Falchetti A 2010 Genetic screening for multiple endocrine neoplasia syndrome type 1 (MEN-1): when and how. F1000 Med Rep;2

4. Trump D, Farren B, Wooding C et al (1996) Clinical studies of multiple endocrine neoplasia type 1 (MEN1). QJM 89(9):653–669

5. Flanagan DE, Armitage M, Clein GP et al (1996) Prolactinoma presenting in identical twins with multiple endocrine neoplasia type 1. Clin Endocrinol 45(1):117–120

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