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Two AOS genes attributed to familial exudative vitreoretinopathy with microcephaly: Two case reports

RATIONALE: Familial exudative vitreoretinopathy (FEVR) is an inherited disorder, which is mostly reported to be associated with the mutation of genes involved in the Wnt signaling pathway related to β-catenin. To the best of our knowledge, the involvement of Adams-Oliver syndrome (AOS) genes in FEVR...

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Detalles Bibliográficos
Autores principales: Tao, Zhiyan, Bu, Shaochong, Lu, Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7939203/
https://www.ncbi.nlm.nih.gov/pubmed/33655927
http://dx.doi.org/10.1097/MD.0000000000024633