Identification of Common Mutations Causing Wilson Disease in Egyptian Children
Marwa Mahmoud Abdel-Aziz Alsharkawy;
Abstract
Wilson Disease is caused by excessive accumulation of copper in hepatic and extrahepatic tissues due to defective excretion of copper into bile. As a result, copper accumulates particularly in the liver, kidney, brain, and cornea.
ATP7B gene, is responsi
ATP7B gene, is responsi
Other data
| Title | Identification of Common Mutations Causing Wilson Disease in Egyptian Children | Other Titles | تحديد الطفرات الشائعه المسببه لمرض الويلسون فى الأطفال المصريين | Authors | Marwa Mahmoud Abdel-Aziz Alsharkawy | Keywords | Identification of Common Mutations Causing Wilson Disease in Egyptian Children | Issue Date | 2012 | Description | Wilson Disease is caused by excessive accumulation of copper in hepatic and extrahepatic tissues due to defective excretion of copper into bile. As a result, copper accumulates particularly in the liver, kidney, brain, and cornea. ATP7B gene, is responsi |
Attached Files
| File | Size | Format | |
|---|---|---|---|
| 111293R7294.pdf | 229.66 kB | Adobe PDF | View/Open |
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