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...

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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

Internet

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

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