Items where Author is "Zare-Abdollahi, D."

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Article

(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

This list was generated on Thu Nov 21 17:34:46 2024 +0330.