Novel NR2F1 variants likely disrupt DNA binding: molecular modeling in two cases, review of published cases, genotype–phenotype correlation, and phenotypic expansion of the Bosch–Boonstra–Schaaf optic atrophy syndrome

MLA

Eric W. Klee, et al. “Novel NR2F1 Variants Likely Disrupt DNA Binding: Molecular Modeling in Two Cases, Review of Published Cases, Genotype–phenotype Correlation, and Phenotypic Expansion of the Bosch–Boonstra–Schaaf Optic Atrophy Syndrome.” Molecular Case Studies, vol. 3, Sept. 2017, p. a002162. EBSCOhost, https://doi.org/10.1101/mcs.a002162.

APA

Eric W. Klee, Dusica Babovic-Vuksanovic, Matthew J. Ferber, Raul Urrutia, Charu Kaiwar, Zhiyv Niu, & Michael T. Zimmermann. (2017). Novel NR2F1 variants likely disrupt DNA binding: molecular modeling in two cases, review of published cases, genotype–phenotype correlation, and phenotypic expansion of the Bosch–Boonstra–Schaaf optic atrophy syndrome. Molecular Case Studies, 3, a002162. https://doi.org/10.1101/mcs.a002162

Chicago

Eric W. Klee, Dusica Babovic-Vuksanovic, Matthew J. Ferber, Raul Urrutia, Charu Kaiwar, Zhiyv Niu, and Michael T. Zimmermann. 2017. “Novel NR2F1 Variants Likely Disrupt DNA Binding: Molecular Modeling in Two Cases, Review of Published Cases, Genotype–phenotype Correlation, and Phenotypic Expansion of the Bosch–Boonstra–Schaaf Optic Atrophy Syndrome.” Molecular Case Studies 3 (September): a002162. doi:10.1101/mcs.a002162.