Publications
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Author Title [ Year
] Filters: Author is Støve, Svein Isungset and Keyword is Phenotype [Clear All Filters]
A novel NAA10 variant with impaired acetyltransferase activity causes developmental delay, intellectual disability, and hypertrophic cardiomyopathy. Eur J Hum Genet 26, 1294-1305 (2018).
