Hydrocephalus due to multiple ependymal malformations is caused by mutations in the MPDZ gene

Congenital hydrocephalus is considered as either acquired due to haemorrhage, infection or neoplasia or as of developmental nature and is divided into two subgroups, communicating and obstructive. Congenital hydrocephalus is either syndromic or non-syndromic, and in the latter no cause is found in m...

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Dades bibliogràfiques
Publicat a:Acta Neuropathol Commun
Autors principals: Saugier-Veber, Pascale, Marguet, Florent, Lecoquierre, François, Adle-Biassette, Homa, Guimiot, Fabien, Cipriani, Sara, Patrier, Sophie, Brasseur-Daudruy, Marie, Goldenberg, Alice, Layet, Valérie, Capri, Yline, Gérard, Marion, Frébourg, Thierry, Laquerrière, Annie
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2017
Matèries:
Research
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5412059/
https://ncbi.nlm.nih.gov/pubmed/28460636
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40478-017-0438-4
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