Cite

    Richard, P., Gaudon, K., Andreux, F., Yasaki, E., Prioleau, C., Bauché, S., Barois, A., Ioos, C., Mayer, M., Routon, M. C., Mokhtari, M., Leroy, J. P., Fournier, E., Hainque, B., Koenig, J., Fardeau, M., Eymard, B., & Hantaï, D. (2003). possible founder effect of rapsyn N88K mutation and identification of novel rapsyn mutations in congenital myasthenic syndromes. Journal of medical genetics, 40(6), e81. http://access.bl.uk/ark:/81055/vdc_100136715307.0x000045