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، جلد ۱، شماره ۱، صفحات ۴۳-۴۶
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| عنوان فارسی |
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| چکیده فارسی مقاله |
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| کلیدواژه‌های فارسی مقاله |
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| عنوان انگلیسی |
Novel mutations in ATP7B gene of Wilson's disease in Iranian patients |
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| چکیده انگلیسی مقاله |
Bacground: Wilson's disease is a rare autosomal recessive disorder characterized by toxic accumulation of copper in liver and brain. The disorder is caused by mutations in the ATP7B gene, encoding a copper transporting P-type ATPase. Characterization of the spectrum of mutations in this gene is important both for diagnosis and genetic counseling of the families. Materials and Methods: We enrolled 30 definitely diagnosed patients (ages ranging from 3 to 33). Genomic DNA was extracted from peripheral blood samples. All the exons of the gene were amplified by polymerase chain reaction using specified primers for each exon. The amplification products were then analyzed by direct automated sequencing. Results: 87% of our patients had liver problems while 47% of suffered from neurological problems. In this study we will report the spectrum of mutation found among Iranian families, which are mainly different from other reports. Conclusion: By performing the present study, some new mutations in ATP7B gene, Del C 3696(1232) and S1369L were identified for the first time in Wilson's disease patients. |
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| کلیدواژه‌های انگلیسی مقاله |
Wilson&apos,s disease, ATP7B, mutation detection, Iran |
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| نویسندگان مقاله |
| Iradj Maleki
Department of Internal Medicine, Mazandaran University of Medical Sciences, Sari, Iran
| Mohammad Reza Zali
Research Center of Gastroenterology and Hepatology, Shahid Beheshti University of Medical Science, Tehran, Iran
| Hossein Najm-Abadi
Research Center of Genetics, Rehabilitation University of Tehran, Tehran, Iran
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| نشانی اینترنتی |
http://rmm.mazums.ac.ir/browse.php?a_code=A-10-26-6&slc_lang=en&sid=1 |
| فایل مقاله |
اشکال در دسترسی به فایل - ./files/site1/rds_journals/2735/article-2735-2201310.pdf |
| کد مقاله (doi) |
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| زبان مقاله منتشر شده |
en |
| موضوعات مقاله منتشر شده |
داخلی |
| نوع مقاله منتشر شده |
پژوهشی |
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