Correction: Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population.
Eur J Hum Genet
| Authors | |
| Abstract | An amendment to this paper has been published and can be accessed via a link at the top of the paper. |
| Year of Publication | 2020
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| Journal | Eur J Hum Genet
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| Volume | 28
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| Issue | 4
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| Pages | 532
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| Date Published | 2020 Apr
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| ISSN | 1476-5438
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| DOI | 10.1038/s41431-019-0491-5
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| PubMed ID | 31506600
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| PubMed Central ID | PMC7080772
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| Links |