COMPOUND HETEROZYGOSITY FOR A KNOWN (D250N) AND A NOVEL (E410K) MISSENSE MUTATION IN THE C-TERMINAL DOMAIN OF LIPOPROTEIN-LIPASE CAUSES FAMILIAL CHYLOMICRONEMIA

Authors
WIEBUSCH H FUNKE H BRUIN T BUCHER H VONECKARDSTEIN A KASTELEIN JJP ASSMANN G
Citation
H. Wiebusch et al., COMPOUND HETEROZYGOSITY FOR A KNOWN (D250N) AND A NOVEL (E410K) MISSENSE MUTATION IN THE C-TERMINAL DOMAIN OF LIPOPROTEIN-LIPASE CAUSES FAMILIAL CHYLOMICRONEMIA, Human mutation, 8(4), 1996, pp. 381-383
Citations number
11
Categorie Soggetti
Genetics & Heredity
Journal title
Human mutation → ACNP
ISSN journal
10597794
Volume
8
Issue
4
Year of publication
1996
Pages
381 - 383
Database
ISI
SICI code
1059-7794(1996)8:4<381:CHFAK(>2.0.ZU;2-3