A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy NEM1
Nat Genet
.
1995 Jun;10(2):249.
doi: 10.1038/ng0695-249.
Authors
N G Laing
,
S D Wilton
,
P A Akkari
,
S Dorosz
,
K Boundy
,
C Kneebone
,
P Blumbergs
,
S White
,
H Watkins
,
D R Love
, et al.
PMID:
7663526
DOI:
10.1038/ng0695-249
No abstract available
Publication types
Published Erratum
MeSH terms
Base Sequence
Humans
Molecular Sequence Data
Tropomyosin / genetics*
Substances
Tropomyosin