Kamoun, P <br/><br/>
[A new inherited metabolic disease: delta1-pyrroline 5-carboxylate synthetase deficiency].  [electronic resource] 

 -  Bulletin de l'Academie nationale de medecine  1998 
 - 131-7; discussion 138-9 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0001-4079 
<br/><br/><label>Subjects--Topical Terms: </label><br/>1-Pyrroline-5-Carboxylate Dehydrogenase<br/>Child<br/>Child, Preschool<br/>Cloning, Molecular<br/>Humans<br/>Infant, Newborn<br/>Male<br/>Metabolic Diseases--diagnosis<br/>Mutation<br/>Oxidoreductases Acting on CH-NH Group Donors--deficiency