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Focal segmental glomerulosclerosis and mild intellectual disability in a patient with a novel de novo truncating TRIM8 mutation.
Eur J Med Genet. 2020 Sep;63(9):103972. doi: 10.1016/j.ejmg.2020.103972. Epub 2020 Jun 10.
Eur J Med Genet. 2020.
PMID: 32531461
Antineurofascin IgG2-associated paediatric autoimmune nodopathy.
Harris RE, Atherton M, Naude JTW, Bird-Lieberman GA, Ramdas S, Fehmi J, Rinaldi S, Ong MT.
Harris RE, et al. Among authors: naude jtw.
Dev Med Child Neurol. 2023 Aug;65(8):1118-1122. doi: 10.1111/dmcn.15493. Epub 2023 Jan 11.
Dev Med Child Neurol. 2023.
PMID: 36631915
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