Associated Papers
Gene Identification for Ocular Congenital Cranial Motor Neuron Disorders Using Human Sequencing, Zebrafish Screening, and Protein Binding Microarrays.
Jurgens JA et al.
Investigative Ophthalmology & Visual Science, 2025
40162949 (PubMed )
Supplement: iovs-66-3-62_s002.xlsx › Supp_Table5
Gene identification for ocular congenital cranial motor neuron disorders using human sequencing, zebrafish screening, and protein binding microarrays.
Jurgens JA et al.
Biorxiv : the Preprint Server for Biology, 2024
39314366 (PubMed )
Supplement: media-2.xlsx › Supp_Table5
Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism.
Kotan LD et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2021
Human Semaphorin 3 Variants Link Melanocortin Circuit Development and Energy Balance.
van der Klaauw AA et al.
Cell, 2019
30661757 (PubMed )
Supplement: mmc1.xlsx › Sheet1
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