Cystinuria in children: Distribution and frequencies of mutations in the SLC3A1 and SLC7A9 genes-Reference-Cited by-同舟云学术

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Cystinuria in children: Distribution and frequencies of mutations in the SLC3A1 and SLC7A9 genes

Published:2002-10 Issue:4 Volume:62 Page:1136-1142
ISSN:0085-2538
Container-title:Kidney International
language:en
Short-container-title:Kidney International

Author:

Botzenhart Elke, ,Vester Udo,Schmidt Christa,Hesse Albrecht,Halber Marc,Wagner Carsten,Lang Florian,Hoyer Peter,Zerres Klaus,Eggermann Thomas

Publisher

Elsevier BV

Subject

Nephrology

Reference16 articles.

1. Urolithiasis in children: The role of hypercalciuria;Stapleton;Pediatr Ann,1987

2. Cystinuria caused by mutations in rBAT, a gene involved in the transport of cystine;Calonge;Nat Genet,1994

3. Non-type I cystinuria caused by mutations in SLC7A9, encoding a subunit (b0,+)AT of rBAT;International Consortium of Cystinuria;Nat Genet,1999

4. Cystinuria subtype and the risk of nephrolithiasis;Goodyer;Kidney Int,1998

5. Renal polyamine excretion, tubular amino acid reabsorption and molecular genetics in cystinuria;Langen;Pediatr Nephrol,2000

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