A novel splice site mutation in a Brazilian patient with hereditary antithrombin deficiency type I

Citation
Lat. Arnaldi et al., A novel splice site mutation in a Brazilian patient with hereditary antithrombin deficiency type I, HUMAN HERED, 49(2), 1999, pp. 119-120
Citations number
3
Categorie Soggetti
Molecular Biology & Genetics
Journal title
HUMAN HEREDITY
ISSN journal
00015652 → ACNP
Volume
49
Issue
2
Year of publication
1999
Pages
119 - 120
Database
ISI
SICI code
0001-5652(1999)49:2<119:ANSSMI>2.0.ZU;2-R