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Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28.
- Published in:
- Human Molecular Genetics, 2002, v. 11, n. 23, p. 2877, doi. 10.1093/hmg/11.23.2877
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- Publication type:
- Article
A Five-Generation Family with Late-Onset Progressive Hereditary Hearing Impairment Due to Cochleosaccular Degeneration.
- Published in:
- Audiology & Neurotology, 1997, v. 2, n. 3, p. 139, doi. 10.1159/000259237
- By:
- Publication type:
- Article
Genotype-phenotype correlations in type 1 Waardenburg syndrome.
- Published in:
- 1996
- By:
- Publication type:
- journal article