Клинический полиморфизм и генетическая характеристика синдромов Дениса-Драша и Фрайзера
Аннотация
Об авторах
О. В. ШатохинаРоссия
М. С. Игнатова
Россия
И. М. Османов
Россия
М. Е. Карманов
Россия
В. В. Невструева
Россия
А. К. Берешева
Россия
Е. В. Васильев
Россия
Е. В. Мелехина
Россия
Е. В. Фокеева
Россия
О. Ю. Турпитко
Россия
О. В. Катышева
Россия
Список литературы
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17. Little M., Holmes G., Bickmore W., van Heyningen V., Hastie N., Wainwright B. DNA binding capacity of the WT1 protein is abolished by Denys-Drash syndrome WT1 point mutations. Hum Mol Genet 1995; 4: 351-358.
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Рецензия
Для цитирования:
Шатохина О.В., Игнатова М.С., Османов И.М., Карманов М.Е., Невструева В.В., Берешева А.К., Васильев Е.В., Мелехина Е.В., Фокеева Е.В., Турпитко О.Ю., Катышева О.В. Клинический полиморфизм и генетическая характеристика синдромов Дениса-Драша и Фрайзера. Нефрология и диализ. 2004;6(4):336-343.
For citation:
Shatokhina O.V., Ignatova M.S., Osmanov I.M., Karmanov M.E., Nevstrueva V.V., Beresheva A.K., Vasil’Ev E.V., Melekhina E.V., Fokeeva E.V., Turpitko O.J., Katysheva O.V. Clinical polymorphism and genetic characteristic of Denys-Drash and Frasier syndromes. Nephrology and Dialysis. 2004;6(4):336-343. (In Russ.)