This page shows the publications Nina Mann has written about Developmental Disabilities.
De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis. Am J Hum Genet. 2021 02 04; 108(2):357-367.
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Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.