Hearing impairment in Stickler syndrome: a systematic review
<p>Abstract</p> <p>Background</p> <p>Stickler syndrome is a connective tissue disorder characterized by ocular, skeletal, orofacial and auditory defects. It is caused by mutations in different collagen genes, namely <it>COL2A1</it>, <it>COL11A1</it&...
Main Authors: | , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2012-10-01
|
Series: | Orphanet Journal of Rare Diseases |
Subjects: | |
Online Access: | http://www.ojrd.com/content/7/1/84 |