Publication | Closed Access
PFN1 mutations are rare in Han Chinese populations with amyotrophic lateral sclerosis
59
Citations
33
References
2013
Year
Neurodegenerative DiseasesAmyotrophic Lateral SclerosisMendelian DisorderGenetic DisorderGeneticsPfn1 MutationsNeurologyDisease Gene IdentificationMedicineHan Chinese PopulationsNeurogenetics
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