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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2021 | 2 |
2023 | 1 |
2024 | 0 |
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Homozygous TFG gene variants expanding the mutational and clinical spectrum of hereditary spastic paraplegia 57 and a review of literature.
J Hum Genet. 2021 Oct;66(10):973-981. doi: 10.1038/s10038-021-00919-9. Epub 2021 Mar 25.
J Hum Genet. 2021.
PMID: 33767317
Griscelli syndrome type 1: a novel pathogenic variant, and review of literature.
Khorram E, Tabatabaiefar MA, Yaghini O, Khorrami M, Yazdani V, Fakhr F, Amini M, Kheirollahi M.
Khorram E, et al.
Mol Genet Genomics. 2023 Mar;298(2):485-493. doi: 10.1007/s00438-022-01971-6. Epub 2023 Jan 18.
Mol Genet Genomics. 2023.
PMID: 36651988
Review.
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Identification of a Missense Variant in the EIF2B3 Gene Causing Vanishing White Matter Disease with Antenatal-Onset but Mild Symptoms and Long-Term Survival.
Khorrami M, Khorram E, Yaghini O, Rezaei M, Hejazifar A, Iravani O, Yazdani V, Riahinezhad M, Kheirollahi M.
Khorrami M, et al.
J Mol Neurosci. 2021 Nov;71(11):2405-2414. doi: 10.1007/s12031-021-01810-0. Epub 2021 Mar 9.
J Mol Neurosci. 2021.
PMID: 33687620
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