WebGlobal Public Health Network - Home. GPHN is a network of individuals and organisations working together to help improve the health of communities around the world, by focussing on evidence-based approaches to reducing harm. GPHN aims to share research and experience across all relevant sectors, and has a particular interest in the roles that ... WebJul 12, 2024 · Please find attached the final report of the independent Global Public Health Intelligence Network (GPHIN) Review Panel. These findings reflect six months of …
Entry - #615501 - MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP ...
WebA number sign (#) is used with this entry because of evidence that molybdenum cofactor deficiency of complementation group C (MOCODC) is caused by homozygous mutation in the GPHN gene on chromosome 14q23.For a general phenotypic description and a discussion of genetic heterogeneity of molybdenum cofactor deficiency, see MOCODA … WebGPHN (KIAA1385) protein expression summary. This gene encodes a neuronal assembly protein that anchors inhibitory neurotransmitter receptors to the postsynaptic cyt oskeleton via high affinity binding to a receptor subunit domain and tubulin dimers. In nonneuronal tissues, the encoded protein is also required for molybdenum cofactor biosynthesis. indian trail service company
10243 - Gene ResultGPHN gephyrin [ (human)] - National …
WebNotice of Funding Opportunity (NOFO) No. SM-22-002 . Assistance Listing Number : 93.696 . Key Dates: Application Deadline . Applications are due by May 17, 2024 . WebJul 12, 2024 · Please find attached the final report of the independent Global Public Health Intelligence Network (GPHIN) Review Panel. These findings reflect six months of interviews, research and deliberations by the Panel. It builds on the initial findings of our interim report, dated February 26, 2024, and presents realistic and actionable … WebThe GPHN gene is associated with autosomal recessive molybdenum cofactor deficiency (MedGen UID: 340761) and autosomal dominant GPHN-related spectrum disorder including seizures, autism and intellectual disability (PMID: 23393157). Additionally, the GPHN gene has preliminary evidence supporting a correlation with autosomal dominant early infantile … lockers wide