{
    "PMID": "10534268",
    "TI": "A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic origin.",
    "JT": "Neurology",
    "BTI": "",
    "DP": "1999-10-22",
    "AU": "Abicht A, Stucka R, Karcagi V, Herczegfalvi A, Horv\u00e1th R, Mortier W, Schara U, Ramaekers V, Jost W, Brunner J, Janssen G, Seidel U, Schlotter B, M\u00fcller-Felber W, Pongratz D, R\u00fcdel R, Lochm\u00fcller H"
}