Homozygous STIL Mutation Causes Holoprosencephaly and Microcephaly in Two Siblings

Holoprosencephaly (HPE) is a frequent congenital malformation of the brain characterized by impaired forebrain cleavage and midline facial anomalies. Heterozygous mutations in 14 genes have been identified in HPE patients that account for only 30% of HPE cases, suggesting the existence of other HPE...

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Detalles Bibliográficos
Autores principales: Mouden, Charlotte, de Tayrac, Marie, Dubourg, Christèle, Rose, Sophie, Carré, Wilfrid, Hamdi-Rozé, Houda, Babron, Marie-Claude, Akloul, Linda, Héron-Longe, Bénédicte, Odent, Sylvie, Dupé, Valérie, Giet, Régis, David, Véronique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4319975/
https://www.ncbi.nlm.nih.gov/pubmed/25658757
http://dx.doi.org/10.1371/journal.pone.0117418

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4319975/
https://www.ncbi.nlm.nih.gov/pubmed/25658757
http://dx.doi.org/10.1371/journal.pone.0117418

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