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Dive into the research topics of 'K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity'. Together they form a unique fingerprint.- Sort by
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Nancy Mokbel, Biljana Ilkovski, Michaela Kreissl, Massimiliano Memo, Cy M. Jeffries, Minttu Marttila, Vilma Lotta Lehtokari, Elina Lemola, Mikaela Grönholm, Nan Yang, Dominique Menard, Pascale Marcorelles, Andoni Echaniz-Laguna, Jens Reimann, Mariz Vainzof, Nicole Monnier, Gianina Ravenscroft, Elyshia McNamara, Kristen J. Nowak, Nigel G. Laing
Research output: Contribution to journal › Article › peer-review