Items where Author is "Zare-Abdollahi, D."
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(2022) Clinical and Molecular Assessment of Iranian Families with Severe Congenital Neutropenia, Identification of HYOU1 and SHOC2 as Potential Novel Gene Defects. IRANIAN JOURNAL OF ALLERGY ASTHMA AND IMMUNOLOGY. pp. 344-354. ISSN 1735-1502 1735-5249 J9 - IRAN J ALLERGY ASTHM
(2019) Identification of PROS1 as a Novel Candidate Gene for Juvenile Retinitis Pigmentosa. International Journal of Molecular and Cellular Medicine. pp. 179-190. ISSN 2251-9637
(2019) MFSD8 gene mutations; evidence for phenotypic heterogeneity. Ophthalmic Genetics. pp. 141-145. ISSN 1381-6810