Sarah Grosch

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Epigenetics (incl. genome methylation and epigenomics)

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Publications (1)

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|Oct 30, 2023

A further case of AFG2B-related neurodevelopmental disorder with hearing loss and microcephaly allows further clarification of pathogenicity of the variant c.1313T>C, p.(Leu438Pro).

Sarah Grosch, Martin Kehrer, Olaf Riess

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