reference/36898676

Predicate	Object
contentType	Journal Article\|Research Support, Non-U.S. Gov't
issn	1664-2392
pageRange	1258982-
startingPage	1258982
bibliographicCitation	Bansal V, Winkelmann BR, Dietrich JW, Boehm BO. Whole-exome sequencing in familial type 2 diabetes identifies an atypical missense variant in the RyR2 gene. Front Endocrinol (Lausanne). 2024;15():1258982. PMID: 38444585; PMCID: PMC10913019.
creator	http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_89953af359789cae0ac7b3d2064ec41f http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_7ed883dd1ae606b08fbaf80c992d794b http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_897df6f482c5e3d2c9d86a703693f762 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_f72df4a1ee1c7c0ad89c13be6c5d5bbb
date	2024-02-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC10913019 https://pubmed.ncbi.nlm.nih.gov/38444585 https://doi.org/10.3389/fendo.2024.1258982
isPartOf	http://rdf.ncbi.nlm.nih.gov/pubchem/journal/39155 https://portal.issn.org/resource/ISSN/1664-2392
language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Whole-exome sequencing in familial type 2 diabetes identifies an atypical missense variant in the RyR2 gene
discusses	http://id.nlm.nih.gov/mesh/M000634046 http://id.nlm.nih.gov/mesh/M0009339 http://id.nlm.nih.gov/mesh/M0029444 http://id.nlm.nih.gov/mesh/M000599440

Total number of triples: 23.