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A neural crest origin for cohesinopathy heart defects
Mutations in subunits or regulators of cohesin cause a spectrum of disorders in humans known as the ‘cohesinopathies’. Cohesinopathies, including the best known example Cornelia de Lange syndrome (CdLS), are characterized by broad spectrum, multifactorial developmental anomalies. Heart defects occur...
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| I publikationen: | Hum Mol Genet |
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| Huvudupphovsmän: | , , , , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Oxford University Press
2015
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4654055/ https://ncbi.nlm.nih.gov/pubmed/26420840 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddv402 |
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