Concepedia

Publication | Closed Access

Genetic analysis of patients with familial and sporadic amyotrophic lateral sclerosis in a Brazilian Research Center

38

Citations

35

References

2016

Year

Abstract

TARDBP and C9orf72 mutations in this cohort were similar to those found in other centres worldwide. VAPB mutation (P56S) was highly prevalent in Brazilian FALS patients.

References

YearCitations

Page 1