Hearing loss in the nonocular Stickler syndrome caused by a COL11A2 mutation.

Admiraal, R J

Hearing loss in the nonocular Stickler syndrome caused by a COL11A2 mutation. [electronic resource] - The Laryngoscope Mar 2000 - 457-61 p. digital

Publication Type: Journal Article

0023-852X

10.1097/00005537-200003000-00025 doi


Adult
Age Factors
Analysis of Variance
Audiometry
Auditory Threshold
Bone Conduction--genetics
Chromosomes, Human, Pair 12--genetics
Cleft Palate--genetics
Connective Tissue Diseases--genetics
Cross-Sectional Studies
Disease Progression
Female
Genetic Linkage--genetics
Hearing Loss, Conductive--genetics
Hearing Loss, Sensorineural--genetics
Humans
Linear Models
Longitudinal Studies
Male
Middle Aged
Mutation--genetics
Myopia--genetics
Otitis Media--genetics
Presbycusis--genetics
Prevalence
Procollagen--genetics
Syndrome