Loss of fibroblast growth factor receptor 2 ligand-binding specificity in Apert syndrome

Craniosynostosis syndromes are autosomal dominant human skeletal diseases that result from various mutations in fibroblast growth factor receptor genes (Fgfrs). Apert syndrome (AS) is one of the most severe craniosynostosis syndromes and is associated with severe syndactyly of the hands and feet and...

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Detalles Bibliográficos

Publicado en:	Proc Natl Acad Sci U S A
Principais autores:	Yu, Kai, Herr, Andrew B., Waksman, Gabriel, Ornitz, David M.
Formato:	Artigo
Idioma:	Inglês
Publicado:	National Academy of Sciences 2000
Assuntos:	Biological Sciences
Acceso en liña:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC18954/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/11121055/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.97.26.14536
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