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GDAP1 gene

Known as: CMT2K, CMT4, GDAP1 
 
National Institutes of Health

Papers overview

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2019
2019
Mutations in genes involved in mitochondrial dynamics (fusion and fission) have been implicated in many peripheral neuropathies… Expand
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2018
2018
Four siblings of consanguineous Bedouin kindred presented at infancy with an autosomal recessive syndrome of congenital… Expand
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2016
2016
Charcot-Marie-Tooth disease type 4C (CMT4C) is an autosomal recessive (AR) demyelinating neuropathy associated to SH3TC2… Expand
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2016
2016
ABSTRACT Alcohol dependence is a severe disorder contributing substantially to the global burden of disease. Despite the… Expand
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2013
2013
Charcot–Marie–Tooth disease (CMT), the most common hereditary neuropathy, has been classified into two types, demyelinating and… Expand
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2013
2013
Objective: To investigate whether mutations in the SURF1 gene are a cause of Charcot-Marie-Tooth (CMT) disease. Methods: We… Expand
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2011
2011
Autosomal recessive Charcot-Marie-Tooth diseases, relatively common in Algeria due to high prevalence of consanguineous marriages… Expand
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2004
2004
Autosomal recessive demyelinating Charcot-Marie-Tooth disease (CMT4), Dejerine-Sottas disease and congenital hypomyelinating… Expand
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2003
2003
By data mining in the sequence of the Corynebacterium glutamicum ATCC 13032 genome, six putative mycolyltransferase genes were… Expand
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Highly Cited
1993
Highly Cited
1993
Autosomal recessive Charcot-Marie-Tooth (CMT) disease (CMT4) is a complex group of severe childhood motor and sensory… Expand
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