Uncovering the mystery of genetic heterogeneity in inherited peripheral neuropathies

Chanjuan Huo; Qinqin Cui; Ge Bai

doi:10.1093/lifemedi/lnad026

Life Medicine ›› 2023, Vol. 2 ›› Issue (4) :2 DOI: 10.1093/lifemedi/lnad026

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Uncovering the mystery of genetic heterogeneity in inherited peripheral neuropathies

Chanjuan Huo ¹^,²^,³
, Qinqin Cui ¹^,²^,³
, Ge Bai ¹^,²^,³^,^†

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Chanjuan Huo, Qinqin Cui, Ge Bai. Uncovering the mystery of genetic heterogeneity in inherited peripheral neuropathies. Life Medicine, 2023, 2(4): 2 DOI:10.1093/lifemedi/lnad026

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References

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[1]	Cui Q, Bi H, Lv Z, et al. Diverse CMT2 neuropathies are linked to aberrant G3BP interactions in stress granules. Cell 2023;186:803–20.e25.

[2]	Vinci P, Esposito C, Perelli SL, et al. Overwork weakness in Charcot-Marie-tooth disease. Arch Phys Med Rehabil 2003;84:825–7.

[3]	Spaulding EL, Hines TJ, Bais P, et al. The integrated stress response contributes to tRNA synthetase-associated peripheral neuropathy. Science 2021;373:1156–61.

[4]	He W, Bai G, Zhou H, et al. CMT2D neuropathy is linked to the neomorphic binding activity of Glycyl-tRNA synthetase. Nature (London) 2015;526:710–4.

[5]	Mo Z, Zhao X, Liu H, et al. Aberrant GlyRS-HDAC6 interaction linked to axonal transport deficits in Charcot-Marie-tooth neuropathy. Nat Commun 2018;9:1007.