Literature for peptidase S08.090: tripeptidyl-peptidase II
(References are filtered for relevance to Mutation. To remove the filter click here. See explanation.)
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Reinthaler,E.M., Graf,E., Zrzavy,T., Wieland,T., Hotzy,C., Kopecky,C., Pferschy,S., Schmied,C., Leutmezer,F., Keilani,M., Lill,C.M., Hoffjan,S., Epplen,J.T., Zettl,U.K., Hecker,M., Deutschlander,A., Meuth,S.G., Ahram,M., Mustafa,B., El-Khateeb,M., Vilarino-Guell,C., Sadovnick,A.D., Zimprich,F., Tomkinson,B., Strom,T., Kristoferitsch,W., Lassmann,H. and Zimprich,A.
TPP2 mutation associated with sterile brain inflammation mimicking MS
Neurol Genet4, e285-e285. PubMed Europe PubMed DOI M -
Stepensky,P., Rensing-Ehl,A., Gather,R., Revel-Vilk,S., Fischer,U., Nabhani,S., Beier,F., Brummendorf,T.H., Fuchs,S., Zenke,S., Firat,E., Pessach,V.M., Borkhardt,A., Rakhmanov,M., Keller,B., Warnatz,K., Eibel,H., Niedermann,G., Elpeleg,O. and Ehl,S.
Early-onset Evans syndrome, immunodeficiency, and premature immunosenescence associated with tripeptidyl-peptidase II deficiency
Blood125, 753-761. PubMed Europe PubMed DOI K M
2018
2015
