Molecular evolution of the human SRPX2 gene that causes brain disorders of the Rolandic and Sylvian speech areas

BACKGROUND: The X-linked SRPX2 gene encodes a Sushi Repeat-containing Protein of unknown function and is mutated in two disorders of the Rolandic/Sylvian speech areas. Since it is linked to defects in the functioning and the development of brain areas for speech production, SRPX2 may thus have parti...

Descripción completa

Detalles Bibliográficos
Autores principales: Royer, Barbara, Soares, Dinesh C, Barlow, Paul N, Bontrop, Ronald E, Roll, Patrice, Robaglia-Schlupp, Andrée, Blancher, Antoine, Levasseur, Anthony, Cau, Pierre, Pontarotti, Pierre, Szepetowski, Pierre
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2151080/
https://www.ncbi.nlm.nih.gov/pubmed/17942002
http://dx.doi.org/10.1186/1471-2156-8-72

Ejemplares similares

Ejemplares similares