association of human mtdna mutations with autism in iranian patients
Authors
abstract
-------------------
similar resources
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...
full textAssociation 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 ...
full textassociation 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...
full textthe past hospitalization and its association with suicide attempts and ideation in patients with mdd and comparison with bmd (depressed type) group
چکیده ندارد.
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...
full textMy Resources
Save resource for easier access later
Journal title:
journal of research in medical sciencesجلد ۱۸، شماره ۱۰، صفحات ۰-۰
Hosted on Doprax cloud platform doprax.com
copyright © 2015-2023