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Lint: kabuki-syndrome

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"In the majority of the patients with Kabuki syndrome, a genetic mutation of MLL2 is identified 1. Other gene mutations causing Kabuki syndrome are reported in the literature including KMT2D inherited in an autosomal dominant manner and KDM6A inherited in an X-linked dominant manner 2."

Line 29:80 · Italics should be used only in exceptional circumstances: '<em>MLL2</em> is identified <sup>1</sup>. Other gene mutations causing Kabuki syndrome are reported in the literature including <em>KMT2D</em> inherited in an autosomal dominant manner and <em>KDM6A</em>'