Zhou, Lin <br/><br/>
Phenotypic characterization of patients with early-onset high myopia due to mutations in   [electronic resource] 

 -  Molecular vision  2018 
 - 560-573 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1090-0535 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Arthritis--diagnosis<br/>Child<br/>Collagen Type II--genetics<br/>Collagen Type XI--genetics<br/>Connective Tissue Diseases--diagnosis<br/>DNA Mutational Analysis<br/>Early Diagnosis<br/>Female<br/>Follow-Up Studies<br/>Genetic Association Studies<br/>Hearing Loss, Sensorineural--diagnosis<br/>Humans<br/>Male<br/>Mutation<br/>Myopia, Degenerative--diagnosis<br/>Pedigree<br/>Phenotype<br/>Retinal Detachment--diagnosis<br/>Young Adult