Maroofian, R., Riemersma, M., Jae, L. T., Zhianabed, N., Willemsen, M. H., Wissink-Lindhout, W. M., . . . van Bokhoven, H. (2017). B3GALNT2 mutations associated with non-syndromic autosomal recessive intellectual disability reveal a lack of genotype–phenotype associations in the muscular dystrophy-dystroglycanopathies. Genome Med.
シカゴスタイル引用形Maroofian, Reza, et al. "B3GALNT2 Mutations Associated With Non-syndromic Autosomal Recessive Intellectual Disability Reveal a Lack of Genotype–phenotype Associations in the Muscular Dystrophy-dystroglycanopathies." Genome Med 2017.
MLA引用形式Maroofian, Reza, et al. "B3GALNT2 Mutations Associated With Non-syndromic Autosomal Recessive Intellectual Disability Reveal a Lack of Genotype–phenotype Associations in the Muscular Dystrophy-dystroglycanopathies." Genome Med 2017.