CAMK2; four genes, one syndrome? Delineation of genotype-phenotype correlations.
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| Title: | CAMK2; four genes, one syndrome? Delineation of genotype-phenotype correlations. |
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| Authors: | Cheung JS; Department of Pediatrics, Erasmus MC, Rotterdam, 3000 CB, the Netherlands., van Woerden GM; Department of Neuroscience, Erasmus MC, Rotterdam, 3015 GD, the Netherlands; The ENCORE Expertise Center for Neurodevelopmental Disorders, Erasmus MC, Rotterdam, 3015 GD, the Netherlands; Department of Clinical Genetics, Erasmus MC, Rotterdam, 3015 GD, the Netherlands; Member of the European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability ERN-ITHACA, the Netherlands. Electronic address: g.vanwoerden@erasmusmc.nl., Veenma DCM; Department of Pediatrics, Erasmus MC, Rotterdam, 3000 CB, the Netherlands; The ENCORE Expertise Center for Neurodevelopmental Disorders, Erasmus MC, Rotterdam, 3015 GD, the Netherlands; Member of the European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability ERN-ITHACA, the Netherlands. |
| Source: | Current opinion in neurobiology [Curr Opin Neurobiol] 2025 Feb; Vol. 90, pp. 102935. Date of Electronic Publication: 2024 Dec 03. |
| Publication Type: | Journal Article; Review |
| Journal Info: | Publisher: Current Biology Country of Publication: England NLM ID: 9111376 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-6882 (Electronic) Linking ISSN: 09594388 NLM ISO Abbreviation: Curr Opin Neurobiol Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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