Literature DB >> 10384375

Cystinylglycinuria: a new neurometabolic disorder?

H Bellet1, F Rejou, C Vallat, H Mion, A Dimeglio.   

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Year:  1999        PMID： 10384375     DOI： 10.1023/a:1005549114594

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  4 in total

1.  Peptiduria presumably caused by aminopeptidase-P deficiency. A new inborn error of metabolism.

Authors:  N Blau; A Niederwieser; D H Shmerling
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982

2.  The occurrence of cystinylglycine in blood plasma.

Authors:  M D Armstrong
Journal:  Biochim Biophys Acta       Date:  1979-05-16

3.  Glutathione-degrading enzymes of microvillus membranes.

Authors:  E M Kozak; S S Tate
Journal:  J Biol Chem       Date:  1982-06-10       Impact factor: 5.157

4.  Cystinylglycine in plasma: diagnostic relevance for pyroglutamic acidemia, homocystinuria, and phenylketonuria.

Authors:  T L Perry; S Hansen
Journal:  Clin Chim Acta       Date:  1981-11-25       Impact factor: 3.786
  4 in total

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