RNASET2-deficient leukoencephalopathy mimicking congenital CMV infection and Aicardi-Goutieres syndrome: a case report with a novel pathogenic variant

MLA

Reyhaneh Kameli, et al. “RNASET2-Deficient Leukoencephalopathy Mimicking Congenital CMV Infection and Aicardi-Goutieres Syndrome: A Case Report with a Novel Pathogenic Variant.” Orphanet Journal of Rare Diseases, vol. 14, no. 1, July 2019, pp. 1–7. EBSCOhost, https://doi.org/10.1186/s13023-019-1155-9.

APA

Reyhaneh Kameli, Man Amanat, Zahra Rezaei, Sareh Hosseionpour, Sedigheh Nikbakht, Houman Alizadeh, Mahmoud Reza Ashrafi, Abdolmajid Omrani, Masoud Garshasbi, & Ali Reza Tavasoli. (2019). RNASET2-deficient leukoencephalopathy mimicking congenital CMV infection and Aicardi-Goutieres syndrome: a case report with a novel pathogenic variant. Orphanet Journal of Rare Diseases, 14(1), 1–7. https://doi.org/10.1186/s13023-019-1155-9

Chicago

Reyhaneh Kameli, Man Amanat, Zahra Rezaei, Sareh Hosseionpour, Sedigheh Nikbakht, Houman Alizadeh, Mahmoud Reza Ashrafi, Abdolmajid Omrani, Masoud Garshasbi, and Ali Reza Tavasoli. 2019. “RNASET2-Deficient Leukoencephalopathy Mimicking Congenital CMV Infection and Aicardi-Goutieres Syndrome: A Case Report with a Novel Pathogenic Variant.” Orphanet Journal of Rare Diseases 14 (1): 1–7. doi:10.1186/s13023-019-1155-9.