LMNA mutations in atypical Werner's syndrome
Lancet
.
2003 Nov 8;362(9395):1585; author reply 1586.
doi: 10.1016/S0140-6736(03)14760-5.
Authors
C Vigouroux
,
F Caux
,
J Capeau
,
S Christin-Maitre
,
A Cohen
PMID:
14615128
DOI:
10.1016/S0140-6736(03)14760-5
No abstract available
Publication types
Comment
Letter
MeSH terms
Adult
Diagnosis, Differential
Humans
Lamin Type B / genetics*
Lipodystrophy / diagnosis
Lipodystrophy / genetics*
Male
Mutation / genetics*
Werner Syndrome / diagnosis
Werner Syndrome / genetics*
Substances
Lamin Type B