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GDAP1 gene

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

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2016
2016
2016
Charcot‐Marie‐Tooth disease type 4C (CMT4C) is an autosomal recessive (AR) demyelinating neuropathy associated to SH3TC2… 
2016
2016
ABSTRACT Alcohol dependence is a severe disorder contributing substantially to the global burden of disease. Despite the… 
2013
2013
Objective: To investigate whether mutations in the SURF1 gene are a cause of Charcot-Marie-Tooth (CMT) disease. Methods: We… 
Review
2013
Review
2013
The prevalence of Charcot‐Marie‐Tooth (CMT) disease or hereditary motor and sensory neuropathy (HMSN) varies in different… 
Highly Cited
2004
Highly Cited
2004
Autosomal recessive demyelinating Charcot-Marie-Tooth disease (CMT4), Dejerine-Sottas disease and congenital hypomyelinating… 
Highly Cited
2003
Highly Cited
2003
By data mining in the sequence of the Corynebacterium glutamicum ATCC 13032 genome, six putative mycolyltransferase genes were… 
Highly Cited
1993
Highly Cited
1993
Autosomal recessive Charcot-Marie-Tooth (CMT) disease (CMT4) is a complex group of severe childhood motor and sensory…