Associated Papers
Research progress in pathogenic genes of hereditary non-syndromic mid-frequency deafness.
Xia W et al.
Frontiers of Medicine, 2016
Non-ocular Stickler syndrome with a novel mutation in COL11A2 diagnosed by massively parallel sequencing in Japanese hearing loss patients.
Iwasa Y et al.
The Annals of Otology, Rhinology, and Laryngology, 2015
Gene symbol: COL11A2. Disease: Otospondylomegaepiphyseal dysplasia.
Uyguner ZO et al.
Human Genetics, 2008
Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locus.
Chen W et al.
Journal of Medical Genetics, 2005
Autosomal recessive disorder otospondylomegaepiphyseal dysplasia is associated with loss-of-function mutations in the COL11A2 gene.
Melkoniemi M et al.
American Journal of Human Genetics, 2000
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