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Biallelic mutations in early-onset, variably progressive neurodegeneration

artículo científico publicado en 2018

Clinical features and tubulin folding cofactor E gene analysis in Iranian patients with Sanjad-Sakati syndrome

artículo científico publicado en 2018

Clinical presentation and natural history of infantile-onset ascending spastic paralysis from three families with an ALS2 founder variant

artículo científico publicado en 2018

Cytogenetic identification of Khuzestani water Buffalo

artículo científico publicado en 2018

Effect of the herbal mixture composed of Aloe Vera, Henna, Adiantum capillus-veneris, and Myrrha on wound healing in streptozotocin-induced diabetic rats

artículo científico publicado en 2016

Gene expression in blood from an individual with β-thalassemia: An RNA sequence analysis

artículo científico publicado en 2019

Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder

scientific article published on 24 October 2019

Loss of the sphingolipid desaturase DEGS1 causes hypomyelinating leukodystrophy

artículo científico publicado en 2019

Mutation Screening of the Krüppel-like Factor 1 Gene in Individuals With Increased Fetal Hemoglobin Referred for Hemoglobinopathy Investigation in South of Iran

artículo científico publicado en 2018

Novel Mutation in the ATP-Binding Cassette Transporter A3 (ABCA3) Encoding Gene Causes Respiratory Distress Syndrome in A Term Newborn in Southwest Iran

artículo científico publicado en 2016

Prenatal diagnosis of a rare de novo 1q22-q25.1 chromosomal deletion syndrome using oligo array CGH

artículo científico publicado en 2018

The First Report of a 290-bp Deletion in β-Globin Gene in the South of Iran

scientific article published on 08 March 2016

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