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Signature MicroRNA expression patterns identified in humans with 22q11.2 deletion/DiGeorge syndrome
Patients with 22q11.2 deletion syndrome have heterogeneous clinical presentations including immunodeficiency, cardiac anomalies, and hypocalcemia. The syndrome arises from hemizygous deletions of up to 3 Mb on chromosome 22q11.2, a region that contains 60 genes and 4 microRNAs. MicroRNAs are importa...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3748608/ https://ncbi.nlm.nih.gov/pubmed/23454892 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.clim.2013.01.011 |
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