The exon 55 deletion in the nebulin gene – One single founder mutation with world-wide occurrence
Vilma‐Lotta Lehtokari(University of Helsinki), Carina Wallgren‐Pettersson(University of Helsinki), Nigel G. Laing(Harry Perkins Institute of Medical Research), Alan H. Beggs(Broad Institute), Elizabeth T. DeChene(Boston Children's Hospital), Mutsumi Kellinsalmi(University of Helsinki), Katarina Pelin(University of Helsinki), Rebecca S. Greenleaf(GfK (United States))
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