A Genome-wide Association Study of Myasthenia Gravis

Carlo Provenzano, Amelia Evoli, Giuseppe Marangi, Mario Sabatelli, Emanuela Bartoccioni, Flavia Scuderi, Alan E. Renton, Hannah A. Pliner, Roberta Ricciardi, Michael A. Nalls, Yevgeniya Abramzon, Sampath Arepalli, Sean Chong, Dena G. Hernandez, Janel O. Johnson, Michelangelo Maestri, J. Raphael Gibbs, Edoardo Errichiello, Adriano Chiò, Gabriella RestagnoMark Macek, Sonja W. Scholz, Andrea Corse, Vinay Chaudhry, Michael Benatar, Richard J. Barohn, April Mcvey, Mamatha Pasnoor, Mazen M. Dimachkie, Julie Rowin, John Kissel, Miriam Freimer, Henry J. Kaminski, Donald B. Sanders, Bernadette Lipscomb, Janice M. Massey, Manisha Chopra, James F. Howard, Wilma J. Koopman, Michael W. Nicolle, Robert M. Pascuzzi, Alan Pestronk, Charlie Wulf, Julaine Florence, Derrick Blackmore, Aimee Soloway, Zaeem Siddiqi, Srikanth Muppidi, Gil Wolfe, David Richman, Michelle M. Mezei, Theresa Jiwa, Joel Oger, Daniel B. Drachman, Bryan J. Traynor

Risultato della ricerca: Contributo in rivistaArticolo in rivistapeer review

84 Citazioni (Scopus)

Abstract

Myasthenia gravis is a chronic, autoimmune, neuromuscular disease characterized by fluctuating weakness of voluntary muscle groups. Although genetic factors are known to play a role in this neuroimmunological condition, the genetic etiology underlying myasthenia gravis is not well understood.
Lingua originaleEnglish
pagine (da-a)N/A-N/A
RivistaJAMA Neurology
Volume2015
DOI
Stato di pubblicazionePubblicato - 2015

Keywords

  • GWAS
  • Miastenia gravis

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