Paper

Tree Display

AceDB Schema

XML Display

Feedback

Paper Report for: Wargon_2012_Neuromuscul.Disord_22_318

Reference

Title: Long-term follow-up of patients with congenital myasthenic syndrome caused by COLQ mutations
Wargon I, Richard P, Kuntzer T, Sternberg D, Nafissi S, Gaudon K, Lebail A, Bauche S, Hantai D and Stojkovic T <2 more author(s)>
Ref: Neuromuscular Disorders, 22:318, 2012 : PubMed

        



Related information



Citations formats

Wargon I, Richard P, Kuntzer T, Sternberg D, Nafissi S, Gaudon K, Lebail A, Bauche S, Hantai D, Fournier E, Eymard B, Stojkovic T (2012)
Long-term follow-up of patients with congenital myasthenic syndrome caused by COLQ mutations
Neuromuscular Disorders 22: 318-24

Wargon I, Richard P, Kuntzer T, Sternberg D, Nafissi S, Gaudon K, Lebail A, Bauche S, Hantai D, Fournier E, Eymard B, Stojkovic T (2012)
Neuromuscular Disorders 22: 318-24



Send your questions or comments to :
Mail to: Nicolas Lenfant, Thierry Hotelier, Yves Bourne, Pascale Marchot and Arnaud Chatonnet.
Please cite: Lenfant 2013 Nucleic.Acids.Res. or Marchot Chatonnet 2012 Prot.Pept Lett.
For technical information about these pages see:
ESTHER Home Page and ACEDB Home Page
AcePerl Lincoln Stein Home Page
webmaster

Acknowledgements and disclaimer