[Information on rare diseases: the Orphanet project]
Rev Med Interne
.
1998:19 Suppl 3:376S-377S.
[Article in French]
Authors
S Aymé
1
,
B Urbero
,
D Oziel
,
E Lecouturier
,
A C Biscarat
Affiliation
1
Inserm SC 11, Villejuif, France.
PMID:
9885859
No abstract available
MeSH terms
Adult
Databases as Topic*
France
Genetic Diseases, Inborn* / epidemiology
Genetic Diseases, Inborn* / physiopathology
Humans
Internet*