Home
Browse
Search
Latest additions
Policies
FAQ
About Open Access
Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s)
Lookup NU author(s)
Dr Rumaisa Bashir
Dr Louise VB Anderson
Jennifer Moss
Stephen Britton
Dr Elizabeth Vafiadaki
Professor Katherine Bushby
Author(s)
Weiler T, Bashir R, Anderson LVB, Davison K, Moss JA, Britton S, Nylen E, Keers S, Vafiadaki E, Greenberg CR, Bushby KMD, Wrogemann K
Publication type
Article
Journal
Human Molecular Genetics
Year
1999
Volume
8
Issue
5
Pages
871-877
ISSN (print)
0964-6906
ISSN (electronic)
1460-2083
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
Publisher
Oxford University Press
URL
http://dx.doi.org/10.1093/hmg/8.5.871
DOI
10.1093/hmg/8.5.871
PubMed id
10196377
Actions