Noncanonical splice‐site variant in peripheral myelin protein 22 gene (PMP22) in a patient with hereditary neuropathy with liability to pressure palsies.

MLA

Kawamoto, Norifumi, et al. “Noncanonical Splice‐site Variant in Peripheral Myelin Protein 22 Gene (PMP22) in a Patient with Hereditary Neuropathy with Liability to Pressure Palsies.” Journal of the Peripheral Nervous System, vol. 28, no. 3, Sept. 2023, pp. 513–17. EBSCOhost, https://doi.org/10.1111/jns.12558.

APA

Kawamoto, N., Hamada, Y., Kobayashi, S., Naruse, H., Ishiura, H., Matsukawa, T., Mitsui, J., Tsuji, S., Sonoo, M., & Toda, T. (2023). Noncanonical splice‐site variant in peripheral myelin protein 22 gene (PMP22) in a patient with hereditary neuropathy with liability to pressure palsies. Journal of the Peripheral Nervous System, 28(3), 513–517. https://doi.org/10.1111/jns.12558

Chicago

Kawamoto, Norifumi, Yuichi Hamada, Shunsuke Kobayashi, Hiroya Naruse, Hiroyuki Ishiura, Takashi Matsukawa, Jun Mitsui, Shoji Tsuji, Masahiro Sonoo, and Tatsushi Toda. 2023. “Noncanonical Splice‐site Variant in Peripheral Myelin Protein 22 Gene (PMP22) in a Patient with Hereditary Neuropathy with Liability to Pressure Palsies.” Journal of the Peripheral Nervous System 28 (3): 513–17. doi:10.1111/jns.12558.