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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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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3891986/ https://ncbi.nlm.nih.gov/pubmed/24401652 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-9-2 |
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