Publication | Open Access
Lack of C9ORF72 coding mutations supports a gain of function for repeat expansions in amyotrophic lateral sclerosis
75
Citations
27
References
2013
Year
Neurodegenerative DiseasesAmyotrophic Lateral SclerosisNeurological DisorderNeurologyNeuroscienceNeurodegenerationRepeat ExpansionsMedicineNeurogenetics
| Year | Citations | |
|---|---|---|
Page 1
Page 1