A Case of Familial Multiple Endocrine Neoplasia Type 1 with a Novel Mutation in theMEN1Gene-Reference-Cited by-同舟云学术

A Case of Familial Multiple Endocrine Neoplasia Type 1 with a Novel Mutation in theMEN1Gene

Published:2011 Issue:2 Volume:26 Page:171
ISSN:2093-596X
Container-title:Endocrinology and Metabolism
language:ko
Short-container-title:Endocrinol Metab

Author:

Kim Min Jung¹,Kim Eun Hee¹,Shin Mi-Seon¹,Kim Joo Hui¹,Na Hee Kyung¹,Park Seong Joon¹,Lee Sang Ah¹,Koh Eun Hee¹,Lee Woo Je¹,Song Ki Ho²,Park Joong-Yeol¹,Lee Ki-Up¹,Kim Gu-Hwan³,Yoo Han-Wook⁴,Kim Min-Seon¹

Affiliation:

1. Department of Internal Medicine, University of Ulsan College of Medicine, Seoul, Korea.

2. Department of Internal Medicine, Konkuk University School of Medicine, Seoul, Korea.

3. Medical Genetics Clinics and Laboratory, University of Ulsan College of Medicine, Seoul, Korea.

4. Department of Pediatrics, University of Ulsan College of Medicine, Seoul, Korea.

Publisher

Korean Endocrine Society

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

https://synapse.koreamed.org/pdf/10.3803/EnM.2011.26.2.171

Reference15 articles.

1. Germline mutations of the MEN1 gene in Korean families with multiple endocrine neoplasia type 1 (MEN1) or MEN1-related disorders

2. A Case of Multiple Endocrine Neoplasia Type 1 with Mutation in MENIN Gene

3. Surgical Management of Hyperinsulinism in the Multiple Endocrine Neoplasia, Type 1 Syndrome

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