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| Year | Number of Results |
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| 2022 | 1 |
| 2023 | 2 |
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Cited In for PMID: 36574751
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TRAPPC9-related neurodevelopmental disorder: Report of a homozygous deletion in TRAPPC9 due to paternal uniparental isodisomy.
Am J Med Genet A. 2023 Apr;191(4):1077-1082. doi: 10.1002/ajmg.a.63100. Epub 2022 Dec 27.
Am J Med Genet A. 2023.
PMID: 36574751
Defective neurite elongation and branching in Nibp/Trappc9 deficient zebrafish and mice.
Hu M, Bodnar B, Zhang Y, Xie F, Li F, Li S, Zhao J, Zhao R, Gedupoori N, Mo Y, Lin L, Li X, Meng W, Yang X, Wang H, Barbe MF, Srinivasan S, Bethea JR, Mo X, Xu H, Hu W.
Hu M, et al.
Int J Biol Sci. 2023 Jun 19;19(10):3226-3248. doi: 10.7150/ijbs.78489. eCollection 2023.
Int J Biol Sci. 2023.
PMID: 37416774
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