Oyanagi, K <br/><br/>
Clinical, biochemical and enzymatic studies in type I hyperprolinemia associated with chromosomal abnormality.  [electronic resource] 

 -  The Tohoku journal of experimental medicine  Apr 1987 
 - 465-75 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0040-8727 
<br/><br/><label>Standard No.: </label>10.1620/tjem.151.465  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Metabolism, Inborn Errors--diet therapy<br/>Chromosome Aberrations<br/>Chromosome Banding<br/>Chromosome Disorders<br/>Chromosomes, Human, Pair 10<br/>Female<br/>Humans<br/>Infant, Newborn<br/>Karyotyping<br/>Liver--enzymology<br/>Proline--blood<br/>Proline Oxidase--deficiency