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Mutations in the calcium-binding motifs of CDH23 and the 35delG mutation inGJB2cause hearing loss in one family

โœ Scribed by Arjan P. de Brouwer; Ronald J. Pennings; Marjolijn Roeters; Peter Van Hauwe; Lisa M. Astuto; Lies H. Hoefsloot; Patrick L. Huygen; Bellinda van den Helm; August F. Deutman; Julie M. Bork; William J. Kimberling; Frans P. Cremers; Cor W. Cremers; Hannie Kremer


Publisher
Springer
Year
2003
Tongue
English
Weight
407 KB
Volume
112
Category
Article
ISSN
0340-6717

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## 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