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Mojgan Rezaei

Yazd University

Missense mutation
Atrophy
Ataxia
Pediatrics
Encephalopathy

2

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1

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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.

2021 Journal of Human Genetics
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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.

2021 Journal of Molecular Neuroscience
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