Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a U2HR mutation

Identification of a novel frameshift mut

Identification of a novel frameshift mutation in the DFNB31/WHRN gene in a Tunisian consanguineous family with hereditary non-syndromic recessive hearing loss

✍ Abdelaziz Tlili; Ilhem Charfedine; Imed Lahmar; Zaineb Benzina; Ben Amor Mohamed 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 65 KB 👁 1 views

## Communicated by Henrik Dahl Approximately 80% of hereditary hearing loss is non-syndromic. Non-syndromic deafness is the most genetically heterogeneous trait. The most common and severe form of hereditary hearing impairment is autosomal recessive non-syndromic hearing loss (ARNSHL), accounting f