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. Author manuscript; available in PMC: 2021 Jun 1.
Published in final edited form as: Am J Med Genet B Neuropsychiatr Genet. 2020 Apr 8;183(4):227–233. doi: 10.1002/ajmg.b.32781

FIGURE 1.

FIGURE 1

Counts of phenotypic manifestations for loss of function versus duplication. Venn diagram depicting the number of MYT1L loss of function (lof, red) and duplication (dup, blue) cases presenting with each individual phenotype of interest, including their overlap; color coding matches that of Supporting Information Data S1, where comprehensive patient and reference data can be found