Distinct cerebellar foliation anomalies in a CHD7 haploinsufficient mouse model of CHARGE syndrome

Mutations in the gene encoding the ATP dependent chromatin‐remodeling factor, CHD7 are the major cause of CHARGE (Coloboma, Heart defects, Atresia of the choanae, Retarded growth and development, Genital‐urinary anomalies, and Ear defects) syndrome. Neurodevelopmental defects and a range of neurolog...

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Detalles Bibliográficos
Autores principales: Whittaker, Danielle E., Kasah, Sahrunizam, Donovan, Alex P. A., Ellegood, Jacob, Riegman, Kimberley L. H., Volk, Holger A., McGonnell, Imelda, Lerch, Jason P., Basson, M. Albert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5765394/
https://www.ncbi.nlm.nih.gov/pubmed/29168327
http://dx.doi.org/10.1002/ajmg.c.31595

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5765394/
https://www.ncbi.nlm.nih.gov/pubmed/29168327
http://dx.doi.org/10.1002/ajmg.c.31595

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