CLINICAL CHARACTERIZATION AND MOLECULAR-BASIS FOR THE APOPTOTIC DEFECT IN HUMANS WITH FAS MUTATIONS (CANALE-SMITH-SYNDROME)

Citation
Ak. Vaishnaw et al., CLINICAL CHARACTERIZATION AND MOLECULAR-BASIS FOR THE APOPTOTIC DEFECT IN HUMANS WITH FAS MUTATIONS (CANALE-SMITH-SYNDROME), Arthritis and rheumatism, 41(9), 1998, pp. 1511-1511
Citations number
NO
Categorie Soggetti
Rheumatology
Journal title
ISSN journal
00043591
Volume
41
Issue
9
Year of publication
1998
Supplement
S
Pages
1511 - 1511
Database
ISI
SICI code
0004-3591(1998)41:9<1511:CCAMFT>2.0.ZU;2-6