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PRX gene

Known as: KIAA1620, PERIAXIN, PRX 
National Institutes of Health

Papers overview

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2016
2016
Periaxin is expressed in mammalian Schwann cells and lens fiber cells, and has been identified in a screen for cytoskeleton… 
2016
2016
Periaxin, a protein of noncompact myelin, is specifically expressed in the peripheral nervous system (PNS). There are two protein… 
2014
2014
Wallerian degeneration is a subject of major interest in neuroscience. A large number of genes are differentially regulated… 
2013
2013
Charcot-Marie-Tooth (CMT) disease is an inherited peripheral neuropathy caused by mutations in more than 30 different genes. One… 
Highly Cited
2008
Highly Cited
2008
Autosomal recessive Charcot-Marie-Tooth syndrome (AR-CMT) is often characterised by an infantile disease onset and a severe… 
2008
2008
Background:  Mutations in the periaxin (PRX) gene cause autosomal recessive demyelinating neuropathy Charcot–Marie–Tooth (CMT… 
Review
2005
Review
2005
In some countries with a high prevalence of consanguineous mariage, autosomal recessive inheritance probably accounts for the… 
2004
2004
In some countries with a high prevalence of consanguineous marriages, autosomal recessive inheritance is likely to account for…