Gene identification for ocular congenital cranial motor neuron disorders using human sequencing, zebrafish screening, and protein binding microarrays

Julie A. Jurgens; Paola M. Matos Ruiz; Jessica M. King; Emma E. Foster; Lindsay Berube; Wai‐Man Chan; Brenda J. Barry; Raehoon Jeong; Elisabeth Rothman; Mary C. Whitman; Sarah MacKinnon; Cristina Rivera-Quiles; Brandon M. Pratt; Teresa Easterbrooks; Fiona M. Mensching; Silvio Alessandro Di Gioia; Lynn Pais; Eleina England; Teresa de Berardinis; Adriano Magli; Feray Koc; Kazuhide Asakawa; Koichi Kawakami; Anne O’Donnell‐Luria; David G. Hunter; Caroline D. Robson; Martha L. Bulyk; Elizabeth C. Engle

doi:10.1101/2024.09.12.612713

Abstract

To functionally evaluate novel human sequence-derived candidate genes and variants for unsolved ocular congenital cranial dysinnervation disorders (oCCDDs).

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synapsesocial.com/papers/68e587f4b6db6435875241ef https://doi.org/10.1101/2024.09.12.612713

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Gene identification for ocular congenital cranial motor neuron disorders using human sequencing, zebrafish screening, and protein binding microarrays

Abstract

Discussion

Cite This Study

Gene identification for ocular congenital cranial motor neuron disorders using human sequencing, zebrafish screening, and protein binding microarrays

Abstract

Discussion

Cite This Study

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