LMNA mutations in atypical Werner's syndrome
Lancet
.
2003 Nov 8;362(9395):1585-6; author reply 1586.
doi: 10.1016/S0140-6736(03)14761-7.
Authors
Gisele Bonne
,
Nicolas Levy
PMID:
14615129
DOI:
10.1016/S0140-6736(03)14761-7
No abstract available
Publication types
Comment
Letter
MeSH terms
Humans
Lamin Type B / genetics*
Lipodystrophy / genetics
Mutation / genetics*
Phenotype
Progeria / genetics
Werner Syndrome / diagnosis
Werner Syndrome / genetics*
Substances
Lamin Type B