Items where Author is "Aryani, O."

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(2019) Genetic Analysis of MECP2 Gene in Iranian Patients with Rett Syndrome. Iranian Journal of Child Neurology. pp. 25-34. ISSN 1735-4668

(2015) Detection of Intragenic SMN1 Mutations in Spinal Muscular Atrophy Patients With a Single Copy of SMN1. Journal of Child Neurology. pp. 558-562. ISSN 0883-0738

This list was generated on Tue Dec 3 13:26:04 2024 +0330.