Chrome Extension
WeChat Mini Program
Use on ChatGLM

Novel mutations p.V220E and c.30G>T in menin gene are associated with hereditary predisposition to multiple endocrine neoplasia type 1

Endocrine Abstracts(2016)

Cited 0|Views3
No score
Abstract
Searchable abstracts of presentations at key conferences in endocrinology ISSN 1470-3947 (print) | ISSN 1479-6848 (online)
More
Translated text
Key words
multiple endocrine neoplasia type,menin gene,mutations,hereditary predisposition
AI Read Science
Must-Reading Tree
Example
Generate MRT to find the research sequence of this paper
Chat Paper
Summary is being generated by the instructions you defined