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June 4, 2024Annals of Clinical and Translational NeurologyOpen Access

Characterization of a novel TFG variant causing autosomal recessive pure hereditary spastic paraplegia

Cheng‐Tsung Hsiao Tzu‐Yun Tsai Ting‐Yi Shen Yu‐Shuen Tsai Yi‐Chu Liao Yi‐Chung Lee Pei‐Chien Tsai

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Abstract

TFG mutations have previously been implicated in autosomal recessive hereditary spastic paraplegia (HSP), also known as SPG57. This study aimed to investigate the clinical and molecular features of TFG mutations in a Taiwanese HSP cohort.

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Cite This Study

Hsiao et al. (2024) studied this question.

synapsesocial.com/papers/68e664a3b6db6435875f0ac3 https://doi.org/10.1002/acn3.52113

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

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