Mutation in the Monocarboxylate Transporter 12 Gene Affects Guanidinoacetate Excretion but Does Not Cause Glucosuria-Reference-Cited by-同舟云学术

Mutation in the Monocarboxylate Transporter 12 Gene Affects Guanidinoacetate Excretion but Does Not Cause Glucosuria

Published:2015-09-16 Issue:5 Volume:27 Page:1426-1436
ISSN:1046-6673
Container-title:Journal of the American Society of Nephrology
language:en
Short-container-title:JASN

Author:

Dhayat Nasser,Simonin Alexandre,Anderegg Manuel,Pathare Ganesh,Lüscher Benjamin P,Deisl Christine,Albano Giuseppe,Mordasini David,Hediger Matthias A.,Surbek Daniel V.,Vogt Bruno,Sass Jörn Oliver,Kloeckener-Gruissem Barbara,Fuster Daniel G.

Publisher

American Society of Nephrology (ASN)

Subject

Nephrology,General Medicine

Reference23 articles.

1. Juvenile Katarakt assoziiert mit Mikrokornea und Glukosurie: Ein neues Syndrom

2. Mutation of Solute Carrier SLC16A12 Associates with a Syndrome Combining Juvenile Cataract with Microcornea and Renal Glucosuria

3. Juvenile Cataract-Associated Mutation of Solute CarrierSLC16A12Impairs Trafficking of the Protein to the Plasma Membrane

4. The cataract and glucosuria associated monocarboxylate transporter MCT12 is a new creatine transporter

5. Creatine and creatinine metabolism.;Wyss;Physiol Rev,2000

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