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Copy Number Variation in GCK in Patients With Maturity-Onset Diabetes of the Young
PURPOSE: Next generation sequencing (NGS) methods to diagnose maturity-onset diabetes of the young (MODY), a monogenic autosomal dominant cause of diabetes, do not typically detect large-scale copy number variations (CNVs). New techniques may allow assessment for CNVs using output data from targeted...
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| Publicat a: | J Clin Endocrinol Metab |
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| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Endocrine Society
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6594302/ https://ncbi.nlm.nih.gov/pubmed/30912798 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2018-02574 |
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