Thrombophilic Mutations in Iranian Patients With Thrombophilia
نویسندگان
چکیده
منابع مشابه
The Prevalence of Common Mutations in Thrombophilic Patients in Iranian Population with Recurrent Miscarriage
Background and Aims: To date, several factors have been reported in recurrent miscarriage. Genetic mutations are the most important causative factors in women. Fetal thrombotic vasculopathy is a new described placental alteration with varying degrees of involvement and often associated with adverse prenatal outcomes. The diagnosis is made histologically and so is postnatal, which makes it a cha...
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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...
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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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ژورنال
عنوان ژورنال: Laboratory Medicine
سال: 2013
ISSN: 0007-5027,1943-7730
DOI: 10.1309/lmb2hvr9nuqk6wio