Genetical, clinical, and functional analysis of a large international cohort of patients with autosomal recessive congenital ichthyosis due to mutations in NIPAL4.

MLA

Ballin, Nadja, et al. “Genetical, Clinical, and Functional Analysis of a Large International Cohort of Patients with Autosomal Recessive Congenital Ichthyosis Due to Mutations in NIPAL4.” Human Mutation, vol. 40, no. 12, Dec. 2019, pp. 2318–33. EBSCOhost, https://doi.org/10.1002/humu.23883.

APA

Ballin, N., Hotz, A., Bourrat, E., Küsel, J., Oji, V., Bouadjar, B., Brognoli, D., Hickman, G., Heinz, L., Vabres, P., Marrakchi, S., Leclerc, M. S., Irvine, A., Tadini, G., Hamm, H., Has, C., Blume, P. U., Mitter, D., Reitenbach, M., & Hausser, I. (2019). Genetical, clinical, and functional analysis of a large international cohort of patients with autosomal recessive congenital ichthyosis due to mutations in NIPAL4. Human Mutation, 40(12), 2318–2333. https://doi.org/10.1002/humu.23883

Chicago

Ballin, Nadja, Alrun Hotz, Emmanuelle Bourrat, Julia Küsel, Vinzenz Oji, Bakar Bouadjar, Davide Brognoli, et al. 2019. “Genetical, Clinical, and Functional Analysis of a Large International Cohort of Patients with Autosomal Recessive Congenital Ichthyosis Due to Mutations in NIPAL4.” Human Mutation 40 (12): 2318–33. doi:10.1002/humu.23883.