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Dive into the research topics of 'Identification of 45 novel mutations in the nebulin gene associated with autosomal recessive nemaline myopathy'. Together they form a unique fingerprint.- Sort by
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Vilma Lotta Lehtokari, Katarina Pelin, Maria Sandbacka, Salla Ranta, Kati Donner, Francesco Muntoni, Caroline Sewry, Corrado Angelini, Kate Bushby, Peter Van Den Bergh, Susan Iannaccone, Nigel G. Laing, Carina Wallgren-Pettersson
Research output: Contribution to journal › Article › peer-review