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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Detaylı Bibliyografya
Asıl Yazarlar: Urbizu, Aintzane, Toma, Claudio, Poca, Maria A., Sahuquillo, Juan, Cuenca-León, Ester, Cormand, Bru, Macaya, Alfons
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Public Library of Science 2013
Konular:
Research Article
Online Erişim: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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