By KB In News, ResearchPosted 13. July 2021Variants in clustered protocadherin PCDHGC4 identified as genetic cause of novel neurodevelopmental disorder READ MORE
By KB In News, ResearchPosted 5. July 2021Novel homozygous truncating DNM1 variants identified as genetic cause of developmental and epileptic encephalopathy (DEE) READ MORE
By KB In Gene of the MonthPosted 2. July 2021Gene of the Month – June: CLCN3Autosomal dominant and recessive variants of the CLCN3 gene cause neurodevelopmental disease. Scientists of an international research collaboration studied patients with global developmental [...] READ MORE