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bibliographicCitation Flavigny J, Richard P, Isnard R, Carrier L, Charron P, Bonne G, Forissier J, Desnos M, Dubourg O, Komajda M, Schwartz K, Hainque B. Identification of two novel mutations in the ventricular regulatory myosin light chain gene ( MYL2 ) associated with familial and classical forms of hypertrophic cardiomyopathy. Journal of Molecular Medicine. 1998 Feb 26;76(3-4):208–14. doi: 10.1007/s001090050210.
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date 1998-02-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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title Identification of two novel mutations in the ventricular regulatory myosin light chain gene ( MYL2 ) associated with familial and classical forms of hypertrophic cardiomyopathy
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