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Browsing Universitätsbibliographie by Author "Melchinger, Esther Ursula"

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Haploinsufficiency of KMT2E results in transcriptional changes and leads to non-syndromic intellectual disability

Melchinger, Esther Ursula (2022)
Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy

Riess, Angelika; Haack, Tobias; Melchinger, Esther Ursula; Burchert, Rebecca; Schwarz, Niklas; Weber, Yvonne G. (2019)

Now showing items 1-2 of 2

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