Aerts, L.; Terry, N.A.; Sainath, N.N.; Torres, C.; MartÃn, M.G.; Ramos-Molina, B.; Creemers, J.W.
Novel Homozygous Inactivating Mutation in the PCSK1 Gene in an Infant with Congenital Malabsorptive Diarrhea. Genes 2021, 12, 710.
https://doi.org/10.3390/genes12050710
AMA Style
Aerts L, Terry NA, Sainath NN, Torres C, MartÃn MG, Ramos-Molina B, Creemers JW.
Novel Homozygous Inactivating Mutation in the PCSK1 Gene in an Infant with Congenital Malabsorptive Diarrhea. Genes. 2021; 12(5):710.
https://doi.org/10.3390/genes12050710
Chicago/Turabian Style
Aerts, Laetitia, Nathalie A. Terry, Nina N. Sainath, Clarivet Torres, MartÃn G. MartÃn, Bruno Ramos-Molina, and John W. Creemers.
2021. "Novel Homozygous Inactivating Mutation in the PCSK1 Gene in an Infant with Congenital Malabsorptive Diarrhea" Genes 12, no. 5: 710.
https://doi.org/10.3390/genes12050710
APA Style
Aerts, L., Terry, N. A., Sainath, N. N., Torres, C., MartÃn, M. G., Ramos-Molina, B., & Creemers, J. W.
(2021). Novel Homozygous Inactivating Mutation in the PCSK1 Gene in an Infant with Congenital Malabsorptive Diarrhea. Genes, 12(5), 710.
https://doi.org/10.3390/genes12050710
