Senderek,
Bergmann,
Stendel,
Kirfel,
Verpoorten,
De Jonghe,
Timmerman,
Chrast,
Verheijen,
Lemke,
Battaloglu,
Parman,
Erdem,
Tan,
Topaloglu,
Hahn,
Müller-Felber,
Rizzuto,
Fabrizi,
Stuhrmann,
Rudnik-Schöneborn,
Züchner,
Michael Schröder,
Buchheim,
Straub,
Klepper,
Huehne,
Rautenstrauss,
Büttner,
Nelis,
Zerres,
- Mutations in a gene encoding a novel SH3/TPR domain protein cause autosomal recessive Charcot-Marie-Tooth type 4C neuropathy. Senderek, J., Bergmann, C., Stendel, C., Kirfel, J., Verpoorten, N., De Jonghe, P., Timmerman, V., Chrast, R., Verheijen, M.H., Lemke, G., Battaloglu, E., Parman, Y., Erdem, S., Tan, E., Topaloglu, H., Hahn, A., Müller-Felber, W., Rizzuto, N., Fabrizi, G.M., Stuhrmann, M., Rudnik-Schöneborn, S., Züchner, S., Michael Schröder, J., Buchheim, E., Straub, V., Klepper, J., Huehne, K., Rautenstrauss, B., Büttner, R., Nelis, E., Zerres, K. Am. J. Hum. Genet. (2003)