Phenotypes of two Dutch DFNA3 families with mutations in GJB2. [electronic resource]
Producer: 20110531Description: 191-7 p. digitalISSN:- 0003-4894
- Amino Acid Substitution -- genetics
- Audiometry, Pure-Tone
- Audiometry, Speech
- Child
- Connexin 26
- Connexins -- genetics
- Female
- Hearing Loss, Sensorineural -- genetics
- Humans
- Male
- Mutation, Missense
- Netherlands
- Phenotype
- Temporal Bone -- diagnostic imaging
- Tomography, X-Ray Computed
- Vestibular Function Tests
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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