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Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathy.
Flavigny J, Richard P, Isnard R, Carrier L, Charron P, Bonne G, Forissier JF, Desnos M, Dubourg O, Komajda M, Schwartz K, Hainque B. Flavigny J, et al. Among authors: forissier jf. J Mol Med (Berl). 1998 Mar;76(3-4):208-14. doi: 10.1007/s001090050210. J Mol Med (Berl). 1998. PMID: 9535554
[Incidental discovery of a giant myxoma].
Toban P, Forissier JF, Aupart M, De Muret A, Poitrineau O, Pacouret G, Charbonnier B. Toban P, et al. Among authors: forissier jf. Ann Cardiol Angeiol (Paris). 1998 Jan;47(1):14-8. Ann Cardiol Angeiol (Paris). 1998. PMID: 9772927 French.
15 results