ZEB2, a new candidate gene for asplenia

Primary asplenia is a rare condition with poorly known etiology. Mowat-Wilson syndrome (MWS) is characterized by typical facial dysmorphisms, intellectual disability, microcephaly, epilepsy and the possible presence of internal organ malformations. It is caused by heterozygous mutations or deletions...

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Detalles Bibliográficos
Autores principales: Pons, Linda, Dupuis-Girod, Sophie, Cordier, Marie-Pierre, Edery, Patrick, Rossi, Massimiliano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Letter to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3891986/
https://www.ncbi.nlm.nih.gov/pubmed/24401652
http://dx.doi.org/10.1186/1750-1172-9-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3891986/
https://www.ncbi.nlm.nih.gov/pubmed/24401652
http://dx.doi.org/10.1186/1750-1172-9-2

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