Erratum: Identification of a novel COCH mutation, I109N, highlights the similar clinical features observed in DFNA9 families

Identification of a novel COCH mutation,

Identification of a novel COCH mutation, I109N, highlights the similar clinical features observed in DFNA9 families

✍ Maria Kamarinos; Jim McGill; Michael Lynch; Henrik Dahl 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 136 KB

Hereditary hearing loss is a heterogeneous condition at both the genetic and clinical levels. We have recruited an Australian family with dominant sensorineural nonsyndromic late onset hearing loss. The hearing loss typically begins in the second or third decade of life as a high frequency loss whic