Whole-exome sequencing in familial type 2 diabetes identifies an atypical missense variant in the RyR2 gene

Overview of attention for article published in Frontiers in endocrinology, February 2024

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RT @SPINATeam: Breaking news: In combination with whole-exome sequencing, #SPINA_Carb helped to discover a new form of #MODY #diabetes, cau…

20 Feb 2024

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Breaking news: In combination with whole-exome sequencing, #SPINA_Carb helped to discover a new form of #MODY #diabetes, caused by an atypical missense variant in the #RyR2 gene (coding the the type 2 #ryanodine receptor). https://t.co/HbxxdOXxlS https://t

20 Feb 2024

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New Research: Whole-exome sequencing in familial type 2 diabetes identifies an atypical missense variant in the RyR2 gene: Genome-wide association studies have identified several hundred loci associated with type 2 diabetes mellitus… https://t.co/bf5Ci4FU2

20 Feb 2024

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