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Genetic Analysis of 13 Iranian Families With Leukocyte Adhesion Deficiency Type 1.
J Pediatr Hematol Oncol. 2019 Jan;41(1):e3-e6. doi: 10.1097/MPH.0000000000001221.
J Pediatr Hematol Oncol. 2019.
PMID: 29750748
Characterization of 4 New Mutations in the CYBB Gene in 10 Iranian Families With X-linked Chronic Granulomatous Disease.
Teimourian S, Sazgara F, de Boer M, van Leeuwen K, Roos D, Lashkary S, Chavoshzadeh Z, Nabavi M, Bemanian MH, Isaian A.
Teimourian S, et al. Among authors: lashkary s.
J Pediatr Hematol Oncol. 2018 Jul;40(5):e268-e272. doi: 10.1097/MPH.0000000000001189.
J Pediatr Hematol Oncol. 2018.
PMID: 29702544
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Mutation characterization and heterodimer analysis of patients with leukocyte adhesion deficiency: Including one novel mutation.
Teimourian S, De Boer M, Roos D, Isaian A, Moghanloo E, Lashkary S, Hassani B, Mollanoori H, Babaei V, Azarnezhad A.
Teimourian S, et al. Among authors: lashkary s.
Immunol Lett. 2017 Jul;187:7-13. doi: 10.1016/j.imlet.2017.04.012. Epub 2017 Apr 23.
Immunol Lett. 2017.
PMID: 28445705
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