Mig12, a novel Opitz syndrome gene product partner, is expressed in the embryonic ventral midline and co-operates with Mid1 to bundle and stabilize microtubules

BACKGROUND: Opitz G/BBB syndrome is a genetic disorder characterized by developmental midline abnormalities, such as hypertelorism, cleft palate, and hypospadias. The gene responsible for the X-linked form of this disease, MID1, encodes a TRIM/RBCC protein that is anchored to the microtubules. The a...

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Detalles Bibliográficos
Autores principales: Berti, Caterina, Fontanella, Bianca, Ferrentino, Rosa, Meroni, Germana
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC385223/
https://www.ncbi.nlm.nih.gov/pubmed/15070402
http://dx.doi.org/10.1186/1471-2121-5-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC385223/
https://www.ncbi.nlm.nih.gov/pubmed/15070402
http://dx.doi.org/10.1186/1471-2121-5-9

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