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You searched for: Author/Creator Salehpour, Shadab

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1. A novel SRD5A2 mutation in an Iranian family with sex development disorder. (25th October 2020)

2. A novel SRD5A2 mutation in an Iranian family with sex development disorder. (25th October 2020)

3. Effects of Miglustat on Stabilization of Neurological Disorder in Niemann–Pick Disease Type C: Iranian Pediatric Case Series. (December 2013)

5. Molecular characterization of a large cohort of mucopolysaccharidosis patients: Iran Mucopolysaccharidosis RE‐diagnosis study (IMPRESsion). Issue 4 (3rd February 2022)

6. Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous population. Issue 6 (29th August 2018)