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References
Benson MD, Kincaid JC (2007) The molecular biology and clinical features of amyloid neuropathy. Muscle Nerve 36:411–423
Mak CM, Kwong YL, Lam CW et al (2007) Identification of a novel TTR Gly67Glu mutant and the first case series of familial transthyretin amyloidosis in Hong Kong Chinese. Amyloid 14(4):293–297
Li YF, Ng H, Sun UI, Leong W (2008) Clinical and genetic analysis of three families with familiar amyloid polyneuropathy. Chin Med Sci J 23(4):230–3
Adams D, Suhr OB, Hund E et al (2016) First European consensus for diagnosis, management, and treatment of transthyretin familial amyloid polyneuropathy. Curr Opin Neurol 29(Suppl 1):S14-26
Benson MD (2013) Liver transplantation and transthyretin amyloidosis. Muscle Nerve 47(2):157–162
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SYC and YFZ were involved in conceptualization. SYC contributed to investigation writing—original draft preparation. YFZ was involved in writing—review and editing. All authors have read and agreed to the published version of the manuscript.
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Chen, SY., Zou, YF. FAP due to a rare Gly67Glu mutation in the TTR gene. Acta Neurol Belg (2023). https://doi.org/10.1007/s13760-023-02304-z
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DOI: https://doi.org/10.1007/s13760-023-02304-z