Advances in hereditary deafness
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference56 articles.
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2. Cell and molecular basis of hearing;Lim;Kidney Int,1998
3. Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families;Coucke;Hum Mol Genet,1999
4. KCNE1 mutations cause Jervell and Lange-Nielsen syndrome;Schulze-Bahr;Nat Genet,1997
5. A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome;Neyroud;Nat Genet,1997
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