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WDR5 regulates left-right patterning via chromatin-dependent and -independent functions

Congenital heart disease (CHD) is a major cause of infant mortality and morbidity, yet the genetic causes and mechanisms remain opaque. In a patient with CHD and heterotaxy, a disorder of left-right (LR) patterning, a de novo mutation was identified in the chromatin modifier gene WDR5. WDR5 acts as...

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Bibliografski detalji
Izdano u:Development
Glavni autori: Kulkarni, Saurabh S., Khokha, Mustafa K.
Format: Artigo
Jezik:Inglês
Izdano: The Company of Biologists Ltd 2018
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6288385/
https://ncbi.nlm.nih.gov/pubmed/30377171
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dev.159889
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