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Deafness, Autosomal Dominant 4

Known as: DEAFNESS, AUTOSOMAL DOMINANT 4A, DFNA4, DFNA4A 
 
National Institutes of Health

Papers overview

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2012
2012
Background: Genes evolved in mammals for specialization of hearing. Results: CEA cell adhesion molecule 16 (CEACAM16) is a… Expand
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Highly Cited
2011
Highly Cited
2011
We report on a secreted protein found in mammalian cochlear outer hair cells (OHC) that is a member of the carcinoembryonic… Expand
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2011
2011
Both peripheral neuropathy and distal myopathy are well-established inherited neuromuscular disorders characterized by… Expand
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2005
2005
Mutations in the heavy chain of the class II nonmuscle myosin, MYH14, cause autosomal dominant hearing loss in families linked to… Expand
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Highly Cited
2004
Highly Cited
2004
Myosins have been implicated in various motile processes, including organelle translocation, ion-channel gating, and cytoskeleton… Expand
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Highly Cited
2001
Highly Cited
2001
The mammalian mitochondrial ribosome (mitoribosome) has a highly protein-rich composition with a small sedimentation coefficient… Expand
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2000
2000
Animal mitochondrial protein synthesis systems contain two serine tRNAs (tRNAsSer) corresponding to the codons AGY and UCN, each… Expand
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2000
2000
Stereocilia of the inner ear play an integral role in the mechanotransduction of sound. Their structural support is derived from… Expand
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1995
1995
Inherited hearing impairment can occur either in the presence of other clinical features (syndromic hearing loss, SHL) or in… Expand
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