Wordt geladen...
Identification of a Novel ZIC3 Isoform and Mutation Screening in Patients with Heterotaxy and Congenital Heart Disease
Patients with heterotaxy have characteristic cardiovascular malformations, abnormal arrangement of their visceral organs, and midline patterning defects that result from abnormal left-right patterning during embryogenesis. Loss of function of the transcription factor ZIC3 causes X-linked heterotaxy...
Bewaard in:
| Hoofdauteurs: | , , |
|---|---|
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Public Library of Science
2011
|
| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3157443/ https://ncbi.nlm.nih.gov/pubmed/21858219 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0023755 |
| Tags: |
Voeg label toe
Geen labels, Wees de eerste die dit record labelt!
|