Identification of variants in MBNL1 in patients with a myotonic dystrophy-like phenotype.

MLA

Larsen, Mirjam, et al. “Identification of Variants in MBNL1 in Patients with a Myotonic Dystrophy-like Phenotype.” European Journal of Human Genetics : EJHG, vol. 24, no. 10, Oct. 2016, pp. 1467–72. EBSCOhost, https://doi.org/10.1038/ejhg.2016.41.

APA

Larsen, M., Kress, W., Schoser, B., Hehr, U., Müller, C. R., & Rost, S. (2016). Identification of variants in MBNL1 in patients with a myotonic dystrophy-like phenotype. European Journal of Human Genetics : EJHG, 24(10), 1467–1472. https://doi.org/10.1038/ejhg.2016.41

Chicago

Larsen, Mirjam, Wolfram Kress, Benedikt Schoser, Ute Hehr, Clemens R Müller, and Simone Rost. 2016. “Identification of Variants in MBNL1 in Patients with a Myotonic Dystrophy-like Phenotype.” European Journal of Human Genetics : EJHG 24 (10): 1467–72. doi:10.1038/ejhg.2016.41.