Publication | Closed Access
<scp>Genotype‐phenotype</scp> correlation of K <sub>ATP</sub> channel gene defects causing permanent neonatal diabetes in Indian patients
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Citations
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References
2020
Year
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.
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