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Published Erratum

Role of CAMK2D in neurodevelopment and associated conditions

Pomme M F Rigter et al. Am J Hum Genet. .
No abstract available

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Erratum for

  • Role of CAMK2D in neurodevelopment and associated conditions.
    Rigter PMF, de Konink C, Dunn MJ, Proietti Onori M, Humberson JB, Thomas M, Barnes C, Prada CE, Weaver KN, Ryan TD, Caluseriu O, Conway J, Calamaro E, Fong CT, Wuyts W, Meuwissen M, Hordijk E, Jonkers CN, Anderson L, Yuseinova B, Polonia S, Beysen D, Stark Z, Savva E, Poulton C, McKenzie F, Bhoj E, Bupp CP, Bézieau S, Mercier S, Blevins A, Wentzensen IM, Xia F, Rosenfeld JA, Hsieh TC, Krawitz PM, Elbracht M, Veenma DCM, Schulman H, Stratton MM, Küry S, van Woerden GM. Rigter PMF, et al. Am J Hum Genet. 2024 Feb 1;111(2):364-382. doi: 10.1016/j.ajhg.2023.12.016. Epub 2024 Jan 24. Am J Hum Genet. 2024. PMID: 38272033 Free PMC article.

References

    1. Tolmacheva E.R., Shubina J., Kochetkova T.O., Ushakova L.V., Bokerija E.L., Vasiliev G.S., Mikhaylovskaya G.V., Atapina E.E., Zaretskaya N.V., Sukhikh G.T., et al. CAMK2D De Novo Missense Variant in Patient with Syndromic Neurodevelopmental Disorder: A Case Report. Genes. 2023;14:1177. doi: 10.3390/genes14061177. - DOI - PMC - PubMed

Publication types