Molecular findings and clinical manifestations of 18 Iranian children with Griscelli syndrome type 2: Two novel homozygote mutations in RAB27A gene in a patient.

MLA

Tajik, Shaghayegh, et al. “Molecular Findings and Clinical Manifestations of 18 Iranian Children with Griscelli Syndrome Type 2: Two Novel Homozygote Mutations in RAB27A Gene in a Patient.” Scandinavian Journal of Immunology, vol. 97, no. 5, May 2023, p. e13264. EBSCOhost, https://doi.org/10.1111/sji.13264.

APA

Tajik, S., Badalzadeh, M., Houshmand, M., Alizadeh, Z., Moradi, L., Hamidieh, A. A., Shafiei, A., Heris, J. A., Bahram, S., Molitor, A., Carapito, R., Moin, M., Fazlollahi, M. R., & Pourpak, Z. (2023). Molecular findings and clinical manifestations of 18 Iranian children with Griscelli syndrome type 2: Two novel homozygote mutations in RAB27A gene in a patient. Scandinavian Journal of Immunology, 97(5), e13264. https://doi.org/10.1111/sji.13264

Chicago

Tajik, Shaghayegh, Mohsen Badalzadeh, Massoud Houshmand, Zahra Alizadeh, Leila Moradi, Amir Ali Hamidieh, Alireza Shafiei, et al. 2023. “Molecular Findings and Clinical Manifestations of 18 Iranian Children with Griscelli Syndrome Type 2: Two Novel Homozygote Mutations in RAB27A Gene in a Patient.” Scandinavian Journal of Immunology 97 (5): e13264. doi:10.1111/sji.13264.