Back to search

Article

Multiple Endocrine Neoplasia Type 1: A Chinese Family with a New Germline Mutation(c.201delC) and Detection Errors Due to an Intron Mutation

2020-10-26

Abstract excerpt

<title>Abstract</title> <p>Background: Multiple endocrine neoplasia type 1 (MEN1) is a hereditary cancer syndrome caused by germline mutations in the MEN1 gene located on chromosome 11q13. The three main endocrine tissues affected most frequently by tumors in MEN1 are the parathyroid (95%), enteropancreatic neuroendocrine tissues (50%), and anterior pituitary (40%). The purpose of this study was to report on a Ch...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
112ed03d-94cf-5cf1-8106-0c0fd75b96ea
DOI
10.21203/rs.3.rs-41525/v3
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Multiple Endocrine Neoplasia Type 1: A Chinese Family with a New Germline Mutation(c.201delC) and Detection Errors Due to an Intron MutationDOI 10.21203/rs.3.rs-41525/v3
Select a neighboring publication to make it the new centre.