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Cap disease caused by heterozygous deletion of the β-tropomyosin gene TPM2
V. Lehtokari, C. Ceuterick-De Groote, P. De Jonghe, M. Marttila, Nigel Laing, K. Pelin, C. Wallgren-Pettersson
Research output: Contribution to journal › Article › peer-review
80
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(Scopus)