A common founder mutation in FKRP causes limb girdle muscular dystrophy type 21 (LGMD21) in both Hutterite and European populations (2003)

Author(s): Frosk P, Greenberg CR, Poulin A, Lamont R, Nylen E, Zaik M, Straub V, Bushby K, Frappier D, Roslin NM, Morgan K, Fujiwara TM, Wrogemann K

      • Date: 4-8 November 2003
      • Conference Name: American Journal of Human Genetics: Annual Meeting of the American Society of Human Genetics
      • Volume: 73 (5)
      • Pages: 388 abstract no. 1275
      • Publisher: Cell Press
      • Publication type: Conference Proceedings (inc. abstract)
      • Bibliographic status: Published