{
    "PMID": "10051637",
    "TI": "Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy.",
    "JT": "Proceedings of the National Academy of Sciences of the United States of America",
    "BTI": "",
    "DP": "1999-03-02",
    "AU": "Pelin K, Hilpel\u00e4 P, Donner K, Sewry C, Akkari P A, Wilton S D, Wattanasirichaigoon D, Bang M L, Centner T, Hanefeld F, Odent S, Fardeau M, Urtizberea J A, Muntoni F, Dubowitz V, Beggs A H, Laing N G, Labeit S, de la Chapelle A, Wallgren-Pettersson C"
}