Blehová, B <br/><br/>
Iminoglycinuria in a child in Czechoslovakia.  [electronic resource] 

 -  Humangenetik  Jul 1973 
 - 207-10 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0018-7348 
<br/><br/><label>Standard No.: </label>10.1007/BF00282197  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Metabolism, Inborn Errors--diagnosis<br/>Cerebrospinal Fluid Proteins--analysis<br/>Deafness--genetics<br/>Female<br/>Glycine--metabolism<br/>Humans<br/>Hydroxyproline--metabolism<br/>Infant<br/>Intelligence<br/>Intestinal Absorption<br/>Male<br/>Pedigree<br/>Proline--blood<br/>Seizures--complications<br/>Time Factors