Cite

A new mutation of the lamin A/C gene leading to autosomal dominant axonal neuropathy, muscular dystrophy, cardiac disease, and leuconychia

MLA

G Le Masson, et al. “A New Mutation of the Lamin A/C Gene Leading to Autosomal Dominant Axonal Neuropathy, Muscular Dystrophy, Cardiac Disease, and Leuconychia.” Journal of Medical Genetics, vol. 41, Mar. 2004, p. 29e–29. EBSCOhost, https://doi.org/10.1136/jmg.2003.013383.



APA

G Le Masson, Alain Lagueny, Cyril Goizet, L. Demay, Gisèle Bonne, R. Ben Yaou, E Hermosilla, Marie Rouanet, Xavier Ferrer, S Bouillot, & P. Richard. (2004). A new mutation of the lamin A/C gene leading to autosomal dominant axonal neuropathy, muscular dystrophy, cardiac disease, and leuconychia. Journal of Medical Genetics, 41, 29e–29. https://doi.org/10.1136/jmg.2003.013383



Chicago

G Le Masson, Alain Lagueny, Cyril Goizet, L. Demay, Gisèle Bonne, R. Ben Yaou, E Hermosilla, et al. 2004. “A New Mutation of the Lamin A/C Gene Leading to Autosomal Dominant Axonal Neuropathy, Muscular Dystrophy, Cardiac Disease, and Leuconychia.” Journal of Medical Genetics 41 (March): 29e–29. doi:10.1136/jmg.2003.013383.