Disease: Fragile X Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0016667
Disease: Fragile X Syndrome
Fragile X Syndrome 		0.010 AlteredExpression disease BEFREE Genetic reduction of brain-derived neurotrophic factor in FXS mouse progenitors diminishes the expression of Ca<sub>v</sub> channels and activity-dependent responses, which are associated with increased phosphorylation of the phospholipase C-γ1 site within TrkB receptors and changes of differentiating progenitor subpopulations. 30503263 2018