ZNF469 frequently mutated in the brittle cornea syndrome (BCS) is a single exon gene possibly regulating the expression of several extracellular matrix components

Brittle cornea syndrome (BCS; MIM 229200) is an autosomal recessive generalized connective tissue disorder caused by mutations in ZNF469 and PRDM5. It is characterized by extreme thinning and fragility of the cornea that may rupture in the absence of significant trauma leading to blindness. Keratoco...

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Detalles Bibliográficos
Autores principales: Rohrbach, Marianne, Spencer, Helen L., Porter, Louise F., Burkitt-Wright, Emma M.M., Bürer, Céline, Janecke, Andreas, Bakshi, Madhura, Sillence, David, Al-Hussain, Hailah, Baumgartner, Matthias, Steinmann, Beat, Black, Graeme C.M., Manson, Forbes D.C., Giunta, Cecilia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2013
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3925994/
https://www.ncbi.nlm.nih.gov/pubmed/23680354
http://dx.doi.org/10.1016/j.ymgme.2013.04.014

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3925994/
https://www.ncbi.nlm.nih.gov/pubmed/23680354
http://dx.doi.org/10.1016/j.ymgme.2013.04.014

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