Microcephaly with a disproportionate hippocampal reduction, stem cell loss and neuronal lipid droplet symptoms in Trappc9 KO mice
Author:
Funder
Wellcome Trust
MRC
King Saud University
Publisher
Elsevier BV
Reference73 articles.
1. A novel homozygous variant in TRAPPC2L results in a neurodevelopmental disorder and disrupts TRAPP complex function;Al-Deri;J. Med. Genet.,2021
2. TRAPPC6B biallelic variants cause a neurodevelopmental disorder with TRAPP II and trafficking disruptions;Almousa;Brain,2024
3. A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disability;Amin;BMC Med. Genomics,2022
4. Biallelic loss of TRAPPC9 function links vesicle trafficking pathway to autosomal recessive intellectual disability;Aslanger;J. Hum. Genet.,2022
5. Culturing pyramidal neurons from the early postnatal mouse hippocampus and cortex;Beaudoin;Nat. Protoc.,2012
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1. Chronic pharmacologic manipulation of dopamine transmission ameliorates metabolic disturbance in Trappc9-linked brain developmental syndrome;JCI Insight;2024-06-18
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