Tags: Disease.
Iminoglycinuria sometimes called familial iminoglycinuria is an autosomal recessive disorder of renal tubular transport affecting reabsorption of the amino acid glycine and the imino acids proline and hydroxyproline.
Loading...
This page contains content from the copyrighted Wikipedia article "Iminoglycinuria"; that content is used under the GNU Free Documentation License (GFDL). You may redistribute it, verbatim or modified, providing that you comply with the terms of the GFDL.