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10 p, 379.3 KB Chiari Malformation Type I : a Case-Control Association Study of 58 Developmental Genes / Urbizu, Aintzane (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Toma, Claudio (Universitat de Barcelona. Departament de Genètica) ; Poca Pastor, María Antonia (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Sahuquillo Barris, Juan (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Cuenca-León, Ester (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Cormand, Bru (Universitat de Barcelona. Departament de Genètica) ; Macaya Ruiz, Alfons (Hospital Universitari Vall d'Hebron. Institut de Recerca)
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. [...]
2013 - 10.1371/journal.pone.0057241
PloS one, Vol. 8 Issue 2 (February 2013) , p. e57241  
Detailed record - Creative Commons

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