Mutations in SEPT9 cause hereditary neuralgic amyotrophy
2005 · Nature Genetics · 259 citations
https://doi.org/10.1038/ng1649
Claim or correct this author profile
Claim this profile or suggest corrections to the name, affiliation, bio, photo, or paper titles. Approved changes appear as verified CitedEvidence overlays.
102
Papers
7.8K
Citations
38
h-index
69
i10-index
Eva Nelis is an academic researcher. The author has contributed to research in topics: Hereditary Neurological Disorders & Genetic Neurodegenerative Diseases & Neurological diseases and metabolism. The author has an h-index of 38, co-authored 87 publications.
Click to start Chat