Literature DB >> 15267019

No evidence for a role of SLC7A10 in 19q13 in the etiology of cystinuria.

C Schmidt, U Vester, K Zerres, T Eggermann.   

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Year:  2004        PMID： 15267019     DOI： 10.5414/cnp62071

Source DB:  PubMed          Journal:  Clin Nephrol        ISSN： 0301-0430            Impact factor:   0.975


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  3 in total

1.  Search for mutations in SLC1A5 (19q13) in cystinuria patients.

Authors:  E Brauers; U Vester; K Zerres; T Eggermann
Journal:  J Inherit Metab Dis       Date:  2005       Impact factor: 4.982

Review 2.  Cystinuria: an inborn cause of urolithiasis.

Authors:  Thomas Eggermann; Andreas Venghaus; Klaus Zerres
Journal:  Orphanet J Rare Dis       Date:  2012-04-05       Impact factor: 4.123

3.  No evidence for point mutations in the novel renal cystine transporter AGT1/SLC7A13 contributing to the etiology of cystinuria.

Authors:  Kathrin Olschok; Udo Vester; Sven Lahme; Ingo Kurth; Thomas Eggermann
Journal:  BMC Nephrol       Date:  2018-10-20       Impact factor: 2.388
  3 in total

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