Sequencing analysis of insulin receptor defects and detection of two novel mutations in INSR gene()

por Ardon, O., Procter, M., Tvrdik, T., Longo, N., Mao, R.
Publicado 2014

Creatine transporter deficiency: Novel mutations and functional studies

por Ardon, O., Procter, M., Mao, R., Longo, N., Landau, Y.E., Shilon-Hadass, A., Gabis, L.V., Hoffmann, C., Tzadok, M., Heimer, G., Sada, S., Ben-Zeev, B., Anikster, Y.
Publicado 2016