Type IX collagen is crucial for normal hearing
Author:
Publisher
Elsevier BV
Subject
General Neuroscience
Reference33 articles.
1. Identification of CRYM as a candidate responsible for nonsyndromic deafness, through cDNA microarray analysis of human cochlear and vestibular tissues;Abe;Am J Hum Genet,2003
2. Mutations in the gene encoding KIAA1199 protein, an inner-ear protein expressed in Deiters’ cells and the fibrocytes, as the cause of nonsyndromic hearing loss;Abe;J Hum Genet,2003
3. Identification of mutations in the COL4A5 collagen gene in Alport syndrome;Barker;Science,1990
4. A mutation in the alpha 3 chain of type IX collagen causes autosomal dominant multiple epiphyseal dysplasia with mild myopathy;Bonnemann;Proc Natl Acad Sci USA,2000
5. Pseudoachondroplasia and multiple epiphyseal dysplasia;Briggs;Hum Mutat,2002
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