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Patient-derived iPSC modeling of rare neurodevelopmental disorders: Molecular pathophysiology and prospective therapies
The pathological alterations that manifest during the early embryonic development due to inherited and acquired factors trigger various neurodevelopmental disorders (NDDs). Besides major NDDs, there are several rare NDDs, exhibiting specific characteristics and varying levels of severity triggered d...
Gorde:
| Argitaratua izan da: | Neurosci Biobehav Rev |
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| Egile Nagusiak: | , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
2020
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7962756/ https://ncbi.nlm.nih.gov/pubmed/33370574 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neubiorev.2020.12.025 |
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