Zuazo, Francisca <br/><br/>
The uncommon occurrence of two common inherited disorders in a single patient: a mini case series.  [electronic resource] 

 -  Ophthalmic genetics  10 2018 
 - 631-636 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1744-5094 
<br/><br/><label>Standard No.: </label>10.1080/13816810.2018.1498530  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>ATP-Binding Cassette Transporters--genetics<br/>Adolescent<br/>Aged<br/>Arthritis--complications<br/>Collagen Type XI--genetics<br/>Connective Tissue Diseases--complications<br/>Eye Diseases, Hereditary--complications<br/>Female<br/>Hearing Loss, Sensorineural--complications<br/>Humans<br/>Macular Degeneration--complications<br/>Male<br/>Mutation<br/>Prognosis<br/>Retinal Detachment--complications<br/>Stargardt Disease