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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
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. Among authors: rezaei m.
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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