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The molecular landscape of ASPM mutations in primary microcephaly
BACKGROUND: Autosomal recessive primary microcephaly (MCPH) is a model disease to study human neurogenesis. In affected individuals the brain grows at a reduced rate during fetal life resulting in a small but structurally normal brain and mental retardation. The condition is genetically heterogeneou...
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| Main Authors: | , , , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Publishing Group
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2658750/ https://ncbi.nlm.nih.gov/pubmed/19028728 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2008.062380 |
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