Patton, M A <br/><br/>
An oculocerebral hypopigmentation syndrome: a case report with clinical, histochemical, and ultrastructural findings.  [electronic resource] 

 -  Journal of medical genetics  Feb 1987 
 - 118-22 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0022-2593 
<br/><br/><label>Standard No.: </label>10.1136/jmg.24.2.118  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cerebellar Ataxia--complications<br/>Child, Preschool<br/>Dihydroxyphenylalanine--metabolism<br/>Humans<br/>Intellectual Disability--complications<br/>Male<br/>Monophenol Monooxygenase--metabolism<br/>Myopia--complications<br/>Pigmentation Disorders--complications<br/>Skin--metabolism<br/>Syndrome