Whole-exome sequencing in familial type 2 diabetes identifies an atypical missense variant in the RyR2 gene.
Saved in:
| Title: | Whole-exome sequencing in familial type 2 diabetes identifies an atypical missense variant in the RyR2 gene. |
|---|---|
| Authors: | Bansal V; Department of Pediatrics, University of California San Diego, La Jolla, CA, United States.; Institute of Genomic Medicine, University of California San Diego, La Jolla, CA, United States., Winkelmann BR; ClinPhenomics, Frankfurt am Main, Germany., Dietrich JW; Diabetes, Endocrinology and Metabolism Section, Department of Internal Medicine I, St. Josef Hospital, Ruhr University Hospitals, Bochum, Germany.; Diabetes Center Bochum-Hattingen, St. Elisabeth-Hospital Blankenstein, Hattingen, Germany.; Center for Rare Endocrine Diseases, Ruhr Center for Rare Diseases (CeSER), Ruhr University Bochum and Witten/Herdecke University, Bochum, Germany.; Center for Diabetes Technology, Catholic Hospitals Bochum, Bochum, Germany., Boehm BO; Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore, Singapore. |
| Source: | Frontiers in endocrinology [Front Endocrinol (Lausanne)] 2024 Feb 20; Vol. 15, pp. 1258982. Date of Electronic Publication: 2024 Feb 20 (Print Publication: 2024). |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Frontiers Research Foundation] Country of Publication: Switzerland NLM ID: 101555782 Publication Model: eCollection Cited Medium: Print ISSN: 1664-2392 (Print) Linking ISSN: 16642392 NLM ISO Abbreviation: Front Endocrinol (Lausanne) Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| ISSN: | 1664-2392 |
|---|---|
| DOI: | 10.3389/fendo.2024.1258982 |
