Transcription-terminating mutation in telethonin causing autosomal recessive muscular dystrophy type 2G in a European patient.

MLA

Olivé, Montse, et al. “Transcription-Terminating Mutation in Telethonin Causing Autosomal Recessive Muscular Dystrophy Type 2G in a European Patient.” Neuromuscular Disorders : NMD, vol. 18, no. 12, Dec. 2008, pp. 929–33. EBSCOhost, https://doi.org/10.1016/j.nmd.2008.07.009.

APA

Olivé, M., Shatunov, A., Gonzalez, L., Carmona, O., Moreno, D., Quereda, L. G., Martinez-Matos, J. A., Goldfarb, L. G., & Ferrer, I. (2008). Transcription-terminating mutation in telethonin causing autosomal recessive muscular dystrophy type 2G in a European patient. Neuromuscular Disorders : NMD, 18(12), 929–933. https://doi.org/10.1016/j.nmd.2008.07.009

Chicago

Olivé, Montse, Alexey Shatunov, Laura Gonzalez, Olga Carmona, Dolores Moreno, Lidia Gonzalez Quereda, J A Martinez-Matos, Lev G Goldfarb, and Isidro Ferrer. 2008. “Transcription-Terminating Mutation in Telethonin Causing Autosomal Recessive Muscular Dystrophy Type 2G in a European Patient.” Neuromuscular Disorders : NMD 18 (12): 929–33. doi:10.1016/j.nmd.2008.07.009.