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A novel intragenic deletion in OPHN1 in a Japanese patient with Dandy-Walker malformation
Dandy-Walker malformation (DWM) is a rare congenital malformation defined by hypoplasia of the cerebellar vermis and cystic dilatation of the fourth ventricle. Oligophrenin-1 is mutated in X-linked intellectual disability with or without cerebellar hypoplasia. Here, we report a Japanese DWM patient...
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| Udgivet i: | Hum Genome Var |
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| Main Authors: | , , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Nature Publishing Group UK
2018
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6281661/ https://ncbi.nlm.nih.gov/pubmed/30534410 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41439-018-0032-8 |
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