Literature for peptidase M01.001: aminopeptidase N
(References are filtered for relevance to Mutation. To remove the filter click here. See explanation.)
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Willemse,J.L., Chen,D. and Hendriks,D.F.
Major carboxypeptidase N deficiency
Clin Chim Acta389, 181-182. PubMed Europe PubMed DOI M -
Alfalah,M., Krahn,M.P., Wetzel,G., von Horsten,S., Wolke,C., Hooper,N., Kalinski,T., Krueger,S., Naim,H.Y. and Lendeckel,U.
A mutation in aminopeptidase N (CD13) isolated from a patient suffering from leukemia leads to an arrest in the endoplasmic reticulum
J Biol Chem281, 11894-11900. PubMed Europe PubMed DOI M -
Dybkaer,K., Kristensen,J.S. and Pedersen,F.S.
Single site polymorphisms and alternative splicing of the human CD13 gene - different splicing frequencies among patients with acute myeloid leukaemia and healthy individuals
Br J Haematol112, 691-696. PubMed Europe PubMed DOI M -
Watt,V.M. and Willard,H.F.
The human aminopeptidase N gene: isolation, chromosome localization, and DNA polymorphism analysis
Hum Genet85, 651-654. PubMed Europe PubMed M
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