Expression of individual mutations and haplotypes in the galactocerebrosidase gene identified by the newborn screening program in New York State and in confirmed cases of Krabbe's disease

MLA

David A. Wenger, et al. “Expression of Individual Mutations and Haplotypes in the Galactocerebrosidase Gene Identified by the Newborn Screening Program in New York State and in Confirmed Cases of Krabbe’s Disease.” Journal of Neuroscience Research, vol. 94, Sept. 2016, pp. 1076–83. EBSCOhost, https://doi.org/10.1002/jnr.23905.

APA

David A. Wenger, Michele Caggana, Joseph J. Orsini, Carlos A. Saavedra-Matiz, Matthew Nichols, & Paola Luzi. (2016). Expression of individual mutations and haplotypes in the galactocerebrosidase gene identified by the newborn screening program in New York State and in confirmed cases of Krabbe’s disease. Journal of Neuroscience Research, 94, 1076–1083. https://doi.org/10.1002/jnr.23905

Chicago

David A. Wenger, Michele Caggana, Joseph J. Orsini, Carlos A. Saavedra-Matiz, Matthew Nichols, and Paola Luzi. 2016. “Expression of Individual Mutations and Haplotypes in the Galactocerebrosidase Gene Identified by the Newborn Screening Program in New York State and in Confirmed Cases of Krabbe’s Disease.” Journal of Neuroscience Research 94 (September): 1076–83. doi:10.1002/jnr.23905.