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...

Full beskrivning

Sparad:
Bibliografiska uppgifter
I publikationen:J Clin Endocrinol Metab
Huvudupphovsmän: Berberich, Amanda J, Huot, Céline, Cao, Henian, McIntyre, Adam D, Robinson, John F, Wang, Jian, Hegele, Robert A
Materialtyp: Artigo
Språk:Inglês
Publicerad: Endocrine Society 2019
Ämnen:
Clinical Research Articles
Länkar: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
Taggar: Lägg till en tagg
Inga taggar, Lägg till första taggen!

Liknande verk