نتایج جستجو برای: iranian novel mutation

تعداد نتایج: 1082005  

Journal: :Iranian journal of neurology 2015
Mohammad Mehdi Heidari Mehri Khatami Shahriar Nafissi Faezeh Hesami-Zokai Afshin Khorrami

BACKGROUND Non-dystrophic myotonias are a heterogeneous set of skeletal, muscular channelopathies, which have been associated with point mutations within sodium channel α-subunit (SCN4A) gene. Because exons 22 and 24 of SCN4A gene are recognized as hot spots for this disease, the purpose of the study is to identify mutation in exons 22 and 24 of SCN4A gene in Iranian non-dystrophic myotonias pa...

A Ghasemi, A Ghotaslou, B Chahardouli, F Nadali, S Abbasian, S Rostami,

Background Myeloproliferative disorders are a group of diseases characterized by increased proliferation of myeloid lineage. In addition to JAK2V617F mutation, several mutations in the c-MPL gene were described in patients with Philadelphia-negative chronic myeloproliferative disorders that could be important in the pathogenesis of diseases. The aim of present study was to investigate the fre...

Journal: :Iranian biomedical journal 2014
Solmaz Jamali Nasim Eskandari Omid Aryani Shadab Salehpour Talieh Zaman Behnam Kamalidehghan Massoud Houshmand

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 mu...

Bita Shalbafan Forouzan Sadeghian Javad Mohammadi-Asl, Maryam Tahmasebi Birgani, Mohammadreza Hajjari, Neda Golchin

Objective(s): Charcot-Marie Tooth disease (CMT) is one of the main inherited causes of motor and sensory neuropathies with variable expressivity and age-of onset. Although more than 70 genes have been identified for CMT, more studies are needed to discover other genes involved in CMT. Introduction of whole exome sequencing (WES) to capture all the exons may help to fin...

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