Fragmentation of filtered proteins and implications for glomerular protein sieving in Fanconi syndrome.
Главные авторы: | Norden, A, Lapsley, M, Lee, P, Pusey, C, Scheinman, S, Tam, F, Thakker, R, Unwin, R, Wrong, O |
---|---|
Формат: | Journal article |
Язык: | English |
Опубликовано: |
2002
|
Схожие документы
-
Glomerular protein sieving and implications for renal failure in Fanconi syndrome.
по: Norden, A, и др.
Опубликовано: (2001) -
Urinary megalin deficiency implicates abnormal tubular endocytic function in Fanconi syndrome.
по: Norden, A, и др.
Опубликовано: (2002) -
Tubular proteinuria defined by a study of Dent's (CLCN5 mutation) and other tubular diseases.
по: Norden, A, и др.
Опубликовано: (2000) -
THE GENE CAUSING DENTS DISEASE, A RENAL FANCONI SYNDROME WITH NEPHROCALCINOSIS AND KIDNEY-STONES, IS ON THE SHORT ARM OF THE X-CHROMOSOME (XP11.22)
по: Thakker, R, и др.
Опубликовано: (1993) -
Dent's disease, a renal Fanconi syndrome with nephrocalcinosis and kidney stones, is associated with a microdeletion involving DXS255 and maps to Xp11.22.
по: Pook, M, и др.
Опубликовано: (1993)