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Defective Vagal Innervation in Murine Tbx1 Mutant Hearts
Haploinsufficiency of the T-box transcription factor TBX1 is responsible for many features of 22q11.2 deletion syndrome. Tbx1 is expressed dynamically in the pharyngeal apparatus during mouse development and Tbx1 homozygous mutants display numerous severe defects including abnormal cranial ganglion...
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| Publicado no: | J Cardiovasc Dev Dis |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6306933/ https://ncbi.nlm.nih.gov/pubmed/30249045 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jcdd5040049 |
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