BMP4 loss-of-function mutations in developmental eye disorders including SHORT syndrome

BMP4 loss-of-function mutations and deletions have been shown to be associated with ocular, digital, and brain anomalies, but due to the paucity of these reports, the full phenotypic spectrum of human BMP4 mutations is not clear. We screened 133 patients with a variety of ocular disorders for BMP4 c...

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Detalles Bibliográficos
Autores principales: Reis, Linda M., Tyler, Rebecca C., Schilter, Kala F., Abdul-Rahman, Omar, Innis, Jeffrey W., Kozel, Beth A., Schneider, Adele S., Bardakjian, Tanya M., Lose, Edward J., Martin, Donna M., Broeckel, Ulrich, Semina, Elena V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2011
Materias:
Original Investigation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3178759/
https://www.ncbi.nlm.nih.gov/pubmed/21340693
http://dx.doi.org/10.1007/s00439-011-0968-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3178759/
https://www.ncbi.nlm.nih.gov/pubmed/21340693
http://dx.doi.org/10.1007/s00439-011-0968-y

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