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Genetic heterogeneity of polymicrogyria: study of 123 patients using deep sequencing
Polymicrogyria is a malformation of cortical development characterized by overfolding and abnormal lamination of the cerebral cortex. Manifestations include epilepsy, speech disturbance and motor and cognitive disability. Causes include acquired prenatal insults and inherited and de novo genetic var...
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| Foilsithe in: | Brain Commun |
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| Main Authors: | , , , , , , , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Oxford University Press
2020
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7878248/ https://ncbi.nlm.nih.gov/pubmed/33604570 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/braincomms/fcaa221 |
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