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Editorial
. 2022 Jul;13(4):261-262.
doi: 10.1159/000525275. Epub 2022 Jul 6.

The Expanding Phenotypic Spectrum of NUP188 Variants Points Toward Multiple Biological Pathways

Editorial

The Expanding Phenotypic Spectrum of NUP188 Variants Points Toward Multiple Biological Pathways

Martin Poot. Mol Syndromol. 2022 Jul.
No abstract available

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References

    1. Bouty A, Ayers KL, Pask A, Heloury Y, Sinclair AH. The Genetic and Environmental Factors Underlying Hypospadias. Sex Dev. 2015;9:239–59. - PMC - PubMed
    1. Del Viso F, Huang F, Myers J, Chalfant M, Zhang Y, Reza N, et al. Congenital Heart Disease Genetics Uncovers Context-Dependent Organization and Function of Nucleoporins at Cilia. Dev Cell. 2016;38:478–92. - PMC - PubMed
    1. Fakhro KA, Choi M, Ware SM, Belmont JW, Towbin JA, Lifton RP, et al. Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning. Proc Natl Acad Sci U S A. 2011;108:2915–20. - PMC - PubMed
    1. Goos JAC, Mathijssen IMJ. Genetic causes of craniosynostosis: an update. Mol Syndromol. 2019;10:6–23. - PMC - PubMed
    1. Haskell GT, Jensen BC, Samsa LA, Marchuk D, Huang W, Skrzynia C, et al. Whole Exome Sequencing Identifies Truncating Variants in Nuclear Envelope Genes in Patients With Cardiovascular Disease. Circ Cardiovasc Genet. 2017;10:e001443. - PMC - PubMed

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