Bone morphogenetic protein 4 (BMP4) loss-of-function variant associated with autosomal dominant Stickler syndrome and renal dysplasia

Stickler syndrome is a genetic disorder that can lead to joint problems, hearing difficulties and retinal detachment. Genes encoding collagen types II, IX and XI are usually responsible, but some families have no causal variant identified. We investigate a variant in the gene encoding growth factor...

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Detalles Bibliográficos
Autores principales: Nixon, Thomas R. W., Richards, Allan, Towns, Laura K., Fuller, Gavin, Abbs, Stephen, Alexander, Philip, McNinch, Annie, Sandford, Richard N., Snead, Martin P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6460578/
https://www.ncbi.nlm.nih.gov/pubmed/30568244
http://dx.doi.org/10.1038/s41431-018-0316-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6460578/
https://www.ncbi.nlm.nih.gov/pubmed/30568244
http://dx.doi.org/10.1038/s41431-018-0316-y

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