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Progressive Cochleovestibular Impairment Caused by a Point Mutation in the COCH Gene at DFNA9

✍ Scribed by Steven J.H. Bom; Martijn H. Kemperman; Yvonne J.M. De Kok; Patrick L.M. Huygen; Wim I.M. Verhagen; Frans P.M. Cremers; Cor W.R.J. Cremers

Book ID
110082095
Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
658 KB
Volume
109
Category
Article
ISSN
0023-852X

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## Abstract Polydactyly is one of the most common forms of congenital malformation in humans, and is displayed by 119 disorders. Crossed polydactyly (CP) is defined as the coexistence of preaxial and postaxial polydactyly with a difference in the axes of polydactyly between the hands and feet. In a