Comprehensive EHMT1 variants analysis broadens genotype-phenotype associations and molecular mechanisms in Kleefstra syndrome
2024 · The American Journal of Human Genetics · 16 citations
https://doi.org/10.1016/j.ajhg.2024.06.008
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15
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11
h-index
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Gertrud Strobl‐Wildemann is an academic researcher from Praxis für Humangenetik. The author has contributed to research in topics: Genetics and Neurodevelopmental Disorders & Epigenetics and DNA Methylation & Cellular transport and secretion. The author has an h-index of 11, co-authored 13 publications.
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