Mathijssen, Inge B <br/><br/>
LONG-TERM FOLLOW-UP OF PATIENTS WITH RETINITIS PIGMENTOSA TYPE 12 CAUSED BY CRB1 MUTATIONS: A Severe Phenotype With Considerable Interindividual Variability.  [electronic resource] 

 -  Retina (Philadelphia, Pa.)  Jan 2017 
 - 161-172 p.  digital 
<br/><br/> Publication Type: Journal Article; Observational Study 
<br/><br/><label>ISSN: </label>1539-2864 
<br/><br/><label>Standard No.: </label>10.1097/IAE.0000000000001127  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Electroretinography<br/>Eye Proteins--genetics<br/>Female<br/>Follow-Up Studies<br/>Humans<br/>Male<br/>Membrane Proteins--genetics<br/>Middle Aged<br/>Mutation<br/>Nerve Tissue Proteins--genetics<br/>Phenotype<br/>Retinitis Pigmentosa--genetics<br/>Tomography, Optical Coherence<br/>Vision Disorders--etiology<br/>Visual Acuity--physiology<br/>Visual Fields--physiology<br/>Young Adult