association of human mtdna mutations with autism in iranian patients

نویسندگان

kazem mousavizadeh

mohammad askari

hajar arian

fazel gourjipour

چکیده

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منابع مشابه

Association of human mtDNA mutations with autism in Iranian patients

Kazem Mousavizadeh1, Mohammad Askari2, Hajar Arian3, Fazel Gourjipour4, Amin R. Nikpour5, Maryam Tavafjadid1, Omid Aryani3, Behnam Kamalidehghan6, Hamid R. Maroof3, Massoud Houshmand3,7 1Department of Molecular Biology, Cellular and Molecular Research Center, Tehran, Iran, 2Department of Biotechnology, College of Allied Medicine, Tehran, Iran, 3Department of Medical Genetic, Special Medical Cen...

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Association of mtDNA mutation with Autism in Iranian patients

The autism spectrum disorders (ASD) are amongst the most heritable complex disorders. Although there have been many efforts to locate the genes associated with ASD risk, many has been remained to be disclosed about the genetics of ASD. Scrutiny's have only disclosed a small number of de novo and inherited variants significantly associated with susceptibility to ASD. These only comprise a small ...

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association of mtdna mutation with autism in iranian patients

the autism spectrum disorders (asd) are amongst the most heritable complex disorders. although there have been many efforts to locate the genes associated with asd risk, many has been remained to be disclosed about the genetics of asd. scrutiny's have only disclosed a small number of de novo and inherited variants significantly associated with susceptibility to asd. these only comprise a s...

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Three Novel Mutations in Iranian Patients with Tay-Sachs Disease

Background: Tay-Sachs disease (TSD), or GM2 gangliosidosis, is a lethal autosomal recessive neurodegenerative disorder, which is caused by a deficiency of beta-hexosaminidase A (HEXA), resulting in lysosomal accumulation of GM2 ganglioside. The aim of this study was to identify the TSD-causing mutations in‌ an Iranian population. Methods: In this study, we examined 31 patients for TSD-causing m...

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عنوان ژورنال:
journal of research in medical sciences

جلد ۱۸، شماره ۱۰، صفحات ۰-۰

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