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&...

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Bibliographic Details
Main Authors: Acke Frederic R E, Dhooge Ingeborg J M, Malfait Fransiska, De Leenheer Els M R
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

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