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6q22.1 microdeletion and susceptibility to pediatric epilepsy
Genomic copy-number variations (CNVs) constitute an important cause of epilepsies and other human neurological disorders. Recent advancement of technologies integrating genome-wide CNV mapping and sequencing is rapidly expanding the molecular field of pediatric neurodevelopmental disorders. In a pre...
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Publicado no: | Eur J Hum Genet |
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Main Authors: | , , , , , , , , , , , , , |
Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
Nature Publishing Group
2015
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4297903/ https://ncbi.nlm.nih.gov/pubmed/24824130 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2014.75 |
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