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Chiari Malformation Type I: A Case-Control Association Study of 58 Developmental Genes
Chiari malformation type I (CMI) is a disorder characterized by hindbrain overcrowding into an underdeveloped posterior cranial fossa (PCF), often causing progressive neurological symptoms. The etiology of CMI remains unclear and is most likely multifactorial. A putative genetic contribution to CMI...
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| Auteurs principaux: | , , , , , , |
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Public Library of Science
2013
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3578784/ https://ncbi.nlm.nih.gov/pubmed/23437350 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0057241 |
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