Works by Galindo, Máximo I.

Missense mutations in the SH3TC2 protein causing Charcot-Marie-Tooth disease type 4C affect its localization in the plasma membrane and endocytic pathway.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 23, p. 4603, doi. 10.1093/hmg/ddp427

By:

• Lupo, Vincenzo;
• Galindo, Máximo I.;
• Martínez-Rubio, Dolores;
• Sevilla, Teresa;
• Vílchez, Juan J.;
• Palau, Francesc;
• Espinós, Carmen

Publication type:

Article