Items where Author is "Sabbagh, Sima"

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Article

(2021) High Prevalence of MMP9 1562C/T Gene Polymorphism in an Iranian Population of Neuromyelitis Optica, A Pilot Study. Gene Reports.

(2021) Using whole exome sequencing in determining the genetic cause of Parkinson disease in an Iranian family. Neurology Asia. pp. 77-83. ISSN 1823-6138

(2019) Association Study between Functional Polymorphisms of MMP9 Gene Promoter and Multiple Sclerosis Susceptibility in an Iranian Population. Iranian Journal of Public Health. pp. 1697-1703. ISSN 2251-6085

This list was generated on Fri Nov 28 02:53:39 2025 +0330.