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Integrative analysis of congenital muscular torticollis: from gene expression to clinical significance
BACKGROUND: Congenital muscular torticollis (CMT) is characterized by thickening and/or tightness of the unilateral sternocleidomastoid muscle (SCM), ending up with torticollis. Our aim was to identify differentially expressed genes (DEGs) and novel protein interaction network modules of CMT, and to...
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| Main Authors: | , , , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3654872/ https://ncbi.nlm.nih.gov/pubmed/23819832 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1755-8794-6-S2-S10 |
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