Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

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
Review
2016
Mitochondria are dynamic organelles that continually move, fuse and divide. The dynamic balance of fusion and fission of… Expand
2016
2016
ABSTRACT Alcohol dependence is a severe disorder contributing substantially to the global burden of disease. Despite the… Expand
2016
2016
Charcot‐Marie‐Tooth disease type 4C (CMT4C) is an autosomal recessive (AR) demyelinating neuropathy associated to SH3TC2… Expand
2013
2013
Objective: To investigate whether mutations in the SURF1 gene are a cause of Charcot-Marie-Tooth (CMT) disease. Methods: We… Expand
  • figure 1
  • table 1
  • table 2
  • figure 2
Review
2013
Review
2013
The prevalence of Charcot‐Marie‐Tooth (CMT) disease or hereditary motor and sensory neuropathy (HMSN) varies in different… Expand
2011
2011
Autosomal recessive Charcot-Marie-Tooth diseases, relatively common in Algeria due to high prevalence of consanguineous marriages… Expand
  • table 1
  • figure 1
  • figure 2
  • figure 3
  • figure 4
2011
2011
Charcot-Marie-Tooth (CMT) disease is a category of hereditary neuropathy. Rather than 1 disease, CMT is a syndrome of several… Expand
Highly Cited
2004
Highly Cited
2004
Autosomal recessive demyelinating Charcot-Marie-Tooth disease (CMT4), Dejerine-Sottas disease and congenital hypomyelinating… Expand
  • figure 1
  • figure 2
  • table 2
  • figure 3
  • figure 4
Highly Cited
2003
Highly Cited
2003
By data mining in the sequence of the Corynebacterium glutamicum ATCC 13032 genome, six putative mycolyltransferase genes were… Expand
  • table 1
  • figure 1
  • figure 2
  • table 2
  • figure 3
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