Skip to main navigation
Skip to search
Skip to main content
Experts@Minnesota Home
Home
Profiles
Research units
University Assets
Projects and Grants
Research output
Datasets
Press/Media
Activities
Fellowships, Honors, and Prizes
Impacts
Search by expertise, name or affiliation
Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophy
Megan L. Landsverk
, Elizabeth K. Ruzzo
, Heather C. Mefford
, Karen Buysse
, Jillian G. Buchan
, Evan E. Eichler
, Elizabeth M. Petty
, Esther A. Peterson
, Dana M. Knutzen
, Karen Barnett
, Martin R. Farlow
, Judy Caress
, Gareth J. Parry
, Dianna Quan
, Kathy L. Gardner
, Ming Hong
, Zachary Simmons
, Thomas D. Bird
, Phillip F. Chance
, Mark C. Hannibal
Research output
:
Contribution to journal
›
Article
›
peer-review
24
Scopus citations
Overview
Fingerprint
Fingerprint
Dive into the research topics of 'Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophy'. Together they form a unique fingerprint.
Sort by
Weight
Alphabetically
Keyphrases
North America
100%
American Family
100%
Duplication
100%
Founder Effect
100%
SEPT9 Gene
100%
Hereditary Neuralgic Amyotrophy
100%
SEPT9
66%
Exon
50%
Founder Haplotype
33%
Molecular Analysis
16%
Pedigree Analysis
16%
Pedigree
16%
Point mutation
16%
Transcript Variants
16%
Immunoblotting
16%
Protein Isoforms
16%
Autosomal Dominant Disorder
16%
Common Founder
16%
Recurrent Episodes
16%
Brachial Plexus
16%
Proline-rich Region
16%
Sequence mutation
16%
N-terminal Proline
16%
Focal Neuropathy
16%
Biochemistry, Genetics and Molecular Biology
Exon
100%
Founder Effect
100%
Haplotype
66%
Pedigree
66%
Genetics
33%
N-Terminus
33%
Protein Isoform
33%
Molecular Weight
33%
Point Mutation
33%
Autosomal Dominant Inheritance
33%
Immunoblotting
33%
Proline
33%