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Dicarboxylic aminoaciduria

Peghini P, Janzen J, Stoffel W (1997) Glutamate transporter EAAC-1-deficient mice develop dicarboxylic aminoaciduria and behavioral abnormalities but no neurodegeneration. EMBO J 76 3822-3832. [Pg.251]

Swarna M, Rao DN, Reddy PR Dicarboxylic aminoaciduria associated with mental retardation. Hum Genet 1989, 82 299-300... [Pg.308]

Kamoun P, Parvy P, Rabier J. Dicarboxylic aminoaciduria. J Inher Metab Dis 1994, 17 758... [Pg.308]

In the course of studies on aminoaciduria in Fanconi s syndrome, Dent (Dl) isolated from the urine of the subject investigated a simple peptide identified as serylglycylglycine. Carsten (Cl) found in normal urine several peptides containing in every case one of the dicarboxylic amino acids. He discovered also two tetrapeptides, one of them consisting of equimolar amounts of aspartic acid and glycine, and the second composed of glycine, alanine, and glutamic acid in the ratio 2 1 1. The first of these tetrapeptides was also found in the urine of a patient with rheumatoid arthritis. [Pg.138]

See other pages where Dicarboxylic aminoaciduria is mentioned: [Pg.80]    [Pg.216]    [Pg.303]    [Pg.27]    [Pg.28]    [Pg.302]    [Pg.302]    [Pg.303]    [Pg.307]    [Pg.679]    [Pg.369]    [Pg.80]    [Pg.216]    [Pg.303]    [Pg.27]    [Pg.28]    [Pg.302]    [Pg.302]    [Pg.303]    [Pg.307]    [Pg.679]    [Pg.369]   
See also in sourсe #XX -- [ Pg.216 ]



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