Back to search

Article

Case report: Gitelman Syndrome With Type 2 Diabetes Caused by a New Homozygous Mutation of SLC12A3 (c.1567G>A) and Family Follow-up

2021-11-15

Abstract excerpt

<title>Abstract</title> <p>The authors have requested that this preprint be removed from Research Square.</p>

Topics

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

Identifiers and source

Literature Corpus work
63c7ca64-89d5-58ea-9758-87a766b6268b
DOI
10.21203/rs.3.rs-1035839/v1
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.
Case report: Gitelman Syndrome With Type 2 Diabetes Caused by a New Homozygous Mutation of SLC12A3 (c.1567G&gt;A) and Family Follow-upDOI 10.21203/rs.3.rs-1035839/v1
Select a neighboring publication to make it the new centre.