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<scp>Genotype‐phenotype</scp> correlation of K <sub>ATP</sub> channel gene defects causing permanent neonatal diabetes in Indian patients

16

Citations

14

References

2020

Year

Abstract

This is the first largest study in NDM patients in India demonstrating the importance of K<sub>ATP</sub> channel gene mutation screening in PNDM and efficacy of glibenclamide for Indian patients with K<sub>ATP</sub> -PNDM. The success rate of transfer is more in patients with KCNJ11 mutations compared with those with ABCC8 mutations.

References

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