Weterman, M.A.J., Kuo, M., Kenter, S.B., Gordillo, S., Karjosukarso, D.W., Takase, R., Bronk, M., Oprescu, S., Ruissen, F., Witteveen, R.J.W., Bienfait, H.M.E., Breuning, M., Verhamme, C., Hou, Y.M., Visser, M., Antonellis, A., Baas, F. (2018) Hypermorphic and hypomorphic AARS alleles in patients with CMT2N expand clinical and molecular heterogeneities. Human molecular genetics. 27(23):4036-4050

Weterman, M.A.J., Kuo, M., Kenter, S.B., Gordillo, S., Karjosukarso, D.W., Takase, R., Bronk, M., Oprescu, S., Ruissen, F., Witteveen, R.J.W., Bienfait, H.M.E., Breuning, M., Verhamme, C., Hou, Y.M., Visser, M., Antonellis, A., Baas, F. (2018) Hypermorphic and hypomorphic AARS alleles in patients with CMT2N expand clinical and molecular heterogeneities. Human molecular genetics. 27(23):4036-4050