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Autor:
Yury A. Barbitoff, Diana Alaverdian, Inna G. Tuluzanovskaya, Olga V. Romanova, Mariya S. Balashova, Andrey M. Sarana, Andrey S. Glotov, Sergey G. Scherbak, Tatiana E. Ivashchenko, Aliy Yu. Asanov, Oleg S. Glotov, Tatiana M. Ignatova, Anatoly V. Skalny, Mikhail A. Fedyakov, Natalya A. Zhuchenko, Vladislav S Baranov, Marat I. Filimonov
Publikováno v:
Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS). 59
Background. Wilson’s disease (WD) is a rare inherited disorder caused by mutations in the ATP7B gene resulting in copper accumulation in different organs. However, data on ATP7B mutation spectrum in Russia and worldwide are insufficient and contrad