| Announcements |
|
|
MRU SKIMS Identified Novel mutation in the KCNJ11 gene that predisposes to congenital hyperinsulinemia A rare disease The researchers in MRU, and the Department of Endocrinology, SKIMS in collaboration with MDRF, Chennai, identified a novel homozygous missense mutation in the exon 1 of the KCNJ11 gene, (Chr11.17409532 A>T (GRch37) c.107T>A, p.V36E.) predisposing him to congenital hyperinsulinemia- a rare genetic disorder. The findings from this study were documented and reported in Gene.
2026: Awarded the Centre of Research Excellence (CoRE) Grant by the Department of Health Research (DHR), Ministry of Health & Family Welfare,
|
| Last Updated on Saturday, 18 July 2026 15:36 |