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PMID17825431.
S2CID20637695.
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PMID15464245.
Chadwick BP, Heath SK, Williamson J, et al. (1998). "The human homologue of the ninjurin gene maps to the candidate region of hereditary sensory neuropathy type I (HSNI)". Genomics. 47 (1): 58–63.
doi:
10.1006/geno.1997.5084.
PMID9465296.
Guimarães PE, Fridman C, Gregório SP, et al. (2007). "WITHDRAWN: Association between polymorphisms in genes of inflammatory response and axonal repair with spinal cord injury". Spinal Cord.
doi:
10.1038/sj.sc.3102122.
PMID17893696.
Cardoso CC, Martinez AN, Guimarães PE, et al. (2007). "Ninjurin 1 asp110ala single nucleotide polymorphism is associated with protection in leprosy nerve damage". J. Neuroimmunol. 190 (1–2): 131–8.
doi:
10.1016/j.jneuroim.2007.07.015.
PMID17825431.
S2CID20637695.
Toyama T, Sasaki Y, Horimoto M, et al. (2005). "Ninjurin1 increases p21 expression and induces cellular senescence in human hepatoma cells". J. Hepatol. 41 (4): 637–43.
doi:
10.1016/j.jhep.2004.06.027.
PMID15464245.
Chadwick BP, Heath SK, Williamson J, et al. (1998). "The human homologue of the ninjurin gene maps to the candidate region of hereditary sensory neuropathy type I (HSNI)". Genomics. 47 (1): 58–63.
doi:
10.1006/geno.1997.5084.
PMID9465296.