Further audiovestibular characterization of DFNB77, caused by deleterious variants in LOXHD1, and investigation into the involvement of Fuchs corneal dystrophy. [electronic resource]
Producer: 20191115Description: 221-231 p. digitalISSN:- 1399-0004
- Adolescent
- Adult
- Audiometry
- Carrier Proteins -- genetics
- Child
- Child, Preschool
- Female
- Fuchs' Endothelial Dystrophy -- genetics
- Genetic Association Studies
- Genetic Predisposition to Disease
- Genotype
- Hearing Loss, Sensorineural -- genetics
- Heterozygote
- Humans
- Male
- Middle Aged
- Mutation, Missense
- Pedigree
- Phenotype
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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