Webmail
HelpDesk
Personal Area
RESEARCH
DIAGNOSTICS
TRANSLATION
OUTREACH
Paper Detail
C
IF
Vaz Rodrigues L, Costa F, Marques P, Mendonça C, Rocha J,
Seixas S
Severe a-1 antitrypsin deficiency caused by Q0(Ourém) allele: clinical features, haplotype characterization and history.
Clinical genetics 81: 462-9, 2012.
[Article]
doi:
10.1111/j.1399-0004.2011.01670.x
PMID:
21457231
.
14
3.9
Send Email
From
To
Subject