About this Research Topic
1. This Research Topic aims to provide cutting-edge scientific advances on better understanding of the genetic and molecular bases of MDM, particularly, on uncovering the genetic and cell biology links between the spectrum of clinical phenotypes and known MDM causing gene mutations.
2. Clinical research/trails/reviews that optimize/discuss the current strategies for the genetic diagnosis and/or individualized precision management of MDM are welcome. The clinical research/trails/case reports exploring the novel approaches for diagnosis/management of MDM are particularly welcome.
This special issue focuses on the genetic and molecular bases of MDM, and how the basic and clinical research findings translate to the clinical practices for developing individualized precision management of MDM. We welcome original basic and clinical research, case reports, review and mini-review articles focusing on the following topics:
• Discovering new genetic bases of MDM, particularly, uncovering the genetic links between the spectrum of clinical phenotypes and known MDM causing gene mutations.
• Improving the understanding of molecular bases of MDM, particularly, uncovering the cell biology links between the spectrum of clinical phenotypes and known MDM causing gene mutations.
• Clinical research/trails/reviews that optimize/discuss the current strategies for the genetic diagnosis and/or individualized precision management of MDM. The clinical research/trails/case reports exploring the novel approaches for diagnosis/management of MDM are particularly welcome.
• Clinical research/trails that assess MDM prevalence and the short-term/long-term outcomes of the complications associated with MDM.
Keywords: Monogenic diabetes, Pancreatic beta cells, Gene mutations, Genetic testing, Individualized precision medicine
Important Note: All contributions to this Research Topic must be within the scope of the section and journal to which they are submitted, as defined in their mission statements. Frontiers reserves the right to guide an out-of-scope manuscript to a more suitable section or journal at any stage of peer review.