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Molecular findings and clinical manifestations of 18 Iranian children with Griscelli syndrome type 2: Two novel homozygote mutations in RAB27A gene in a patient.
Tajik S, Badalzadeh M, Houshmand M, Alizadeh Z, Moradi L, Hamidieh AA, Shafiei A, Heris JA, Bahram S, Molitor A, Carapito R, Moin M, Fazlollahi MR, Pourpak Z. Tajik S, et al. Scand J Immunol. 2023 May;97(5):e13264. doi: 10.1111/sji.13264. Epub 2023 Mar 21. Scand J Immunol. 2023. PMID: 37368332 Free article.
The Risk of the Next Child Getting Affected by Chronic Granulomatous Disease in Families with at Least One Autosomal Recessive CGD Child.
Modarresi SZ, Tajik S, Badalzadeh M, Fazlollahi MR, Houshmand M, Maddah M, Alizadeh Z, Nabavi M, Bazargan N, Movahedi M, Pourpak Z. Modarresi SZ, et al. Among authors: tajik s. Iran J Allergy Asthma Immunol. 2023 Feb 20;22(1):119-123. doi: 10.18502/ijaai.v22i1.12014. Iran J Allergy Asthma Immunol. 2023. PMID: 37002626 Free article.
88 results