Literature for peptidase M24.009: aminopeptidase P1
(References are filtered for relevance to Mutation. To remove the filter click here. See explanation.)
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Bae,Y.S., Yoon,S.H., Han,J.Y., Woo,J., Cho,Y.S., Kwon,S.K., Bae,Y.C., Kim,D., Kim,E. and Kim,M.H.
Deficiency of aminopeptidase P1 causes behavioral hyperactivity, cognitive deficits, and hippocampal neurodegeneration
Genes Brain Behav17, 126-138. PubMed Europe PubMed DOI M -
Kaewkiattiyot,S., Honsawek,S., Vejchapipat,P., Chongsrisawat,V. and Poovorawan,Y.
Association of X-prolyl aminopeptidase 1 rs17095355 polymorphism with biliary atresia in Thai children
Hepatol Res41, 1249-1252. PubMed Europe PubMed DOI M
2018
2011
