PTBP1 acts as a dominant repressor of the aberrant tissue‐specific splicing of ISCU in hereditary myopathy with lactic acidosis.

MLA

Rawcliffe, Denise F. R., et al. “PTBP1 Acts as a Dominant Repressor of the Aberrant Tissue‐specific Splicing of ISCU in Hereditary Myopathy with Lactic Acidosis.” Molecular Genetics & Genomic Medicine, vol. 6, no. 6, Nov. 2018, pp. 887–97. EBSCOhost, https://doi.org/10.1002/mgg3.413.

APA

Rawcliffe, D. F. R., Österman, L., Nordin, A., & Holmberg, M. (2018). PTBP1 acts as a dominant repressor of the aberrant tissue‐specific splicing of ISCU in hereditary myopathy with lactic acidosis. Molecular Genetics & Genomic Medicine, 6(6), 887–897. https://doi.org/10.1002/mgg3.413

Chicago

Rawcliffe, Denise F. R., Lennart Österman, Angelica Nordin, and Monica Holmberg. 2018. “PTBP1 Acts as a Dominant Repressor of the Aberrant Tissue‐specific Splicing of ISCU in Hereditary Myopathy with Lactic Acidosis.” Molecular Genetics & Genomic Medicine 6 (6): 887–97. doi:10.1002/mgg3.413.