Two unrelated patients with autosomal dominant omodysplasia and FRIZZLED2 mutations

Presented are two patients with autosomal dominant omodysplasia and mutations in the FZD2 gene. The mutations identified have been recently reported, suggesting the possibility of recurrent mutations. The phenotypes of these patients overlap with what has been previously reported, though intellectua...

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Detalles Bibliográficos
Autores principales: Warren, Hannah E., Louie, Raymond J., Friez, Michael J., Frías, Jaime L., Leroy, Jules G., Spranger, Jürgen W., Skinner, Steven A., Champaigne, Neena L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6230601/
https://www.ncbi.nlm.nih.gov/pubmed/30455931
http://dx.doi.org/10.1002/ccr3.1818

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6230601/
https://www.ncbi.nlm.nih.gov/pubmed/30455931
http://dx.doi.org/10.1002/ccr3.1818

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