Chabaâ, L <br/><br/>
[Oculo-cerebro-renal Lowe syndrome: clinical, biochemical and molecular studies in a Moroccan patient].  [electronic resource] 

 -  Annales de biologie clinique   
 - 53-9 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0003-3898 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Amino Acid Substitution<br/>Animals<br/>Base Sequence<br/>Humans<br/>Infant<br/>Male<br/>Molecular Sequence Data<br/>Morocco<br/>Mutation, Missense<br/>Oculocerebrorenal Syndrome--diagnosis<br/>Phosphoric Monoester Hydrolases--genetics<br/>Sequence Alignment<br/>Sequence Deletion<br/>Sequence Homology, Amino Acid