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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Dades bibliogràfiques

Publicat a:	Proc Natl Acad Sci U S A
Autors principals:	Yu, Kai, Herr, Andrew B., Waksman, Gabriel, Ornitz, David M.
Format:	Artigo
Idioma:	Inglês
Publicat:	National Academy of Sciences 2000
Matèries:	Biological Sciences
Accés en línia:	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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