Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy.

MLA

Ravenscroft, Gianina, et al. “Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy.” American Journal of Human Genetics, vol. 93, no. 1, July 2013, pp. 6–18. EBSCOhost, https://doi.org/10.1016/j.ajhg.2013.05.004.

APA

Ravenscroft, G., Miyatake, S., Lehtokari, V.-L., Todd, E. J., Vornanen, P., Yau, K. S., Hayashi, Y. K., Miyake, N., Tsurusaki, Y., Doi, H., Saitsu, H., Osaka, H., Yamashita, S., Ohya, T., Sakamoto, Y., Koshimizu, E., Imamura, S., Yamashita, M., Ogata, K., … Laing, N. G. (2013). Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy. American Journal of Human Genetics, 93(1), 6–18. https://doi.org/10.1016/j.ajhg.2013.05.004

Chicago

Ravenscroft, Gianina, Satoko Miyatake, Vilma-Lotta Lehtokari, Emily J Todd, Pauliina Vornanen, Kyle S Yau, Yukiko K Hayashi, et al. 2013. “Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy.” American Journal of Human Genetics 93 (1): 6–18. doi:10.1016/j.ajhg.2013.05.004.