Machaczka, M., & Klimkowska, M. (2014). Novel heterozygous c.798C>G and c.1040T>G mutations in the GBA1 gene are associated with a severe phenotype of Gaucher disease type 1. Springer Berlin Heidelberg.
Citação norma ChicagoMachaczka, Maciej, and Monika Klimkowska. Novel Heterozygous C.798C>G and C.1040T>G Mutations in the GBA1 Gene Are Associated With a Severe Phenotype of Gaucher Disease Type 1. Springer Berlin Heidelberg, 2014.
MLA citiranjeMachaczka, Maciej, and Monika Klimkowska. Novel Heterozygous C.798C>G and C.1040T>G Mutations in the GBA1 Gene Are Associated With a Severe Phenotype of Gaucher Disease Type 1. Springer Berlin Heidelberg, 2014.
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