NPY5R, neuropeptide Y receptor Y5, 4889

N. diseases: 32; N. variants: 2
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1334804
Disease: Motor Manifestations
Motor Manifestations
0.010 Biomarker phenotype BEFREE Therefore, the aim of the present study was to analyze different single nucleotide polymorphisms (SNPs) in order to test the possibility that genetic variation in NPY or three of its receptor genes (NPY1R, NPY2R, and NPY5R) may explain some of the variation in AO of HD motor manifestations, in a comprehensive cohort of 487 German HD patients. 24121255 2014