Four novel mutations in APOB causing heterozygous and homozygous familial hypobetalipoproteinemia.

Human mutation

Volumn 22, Issue 2, 2003, Pages 178-

  Whitfield, A J ^a   Marais, A D ^a   Robertson, K ^a   Barrett, P H ^a   van Bockxmeer, F M ^a   Burnett, J R ^a  

^a UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

APOLIPOPROTEIN B;

ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; FEMALE; GENETICS; HETEROZYGOTE; HOMOZYGOTE; HUMAN; HYPOBETALIPOPROTEINEMIA; MALE; MIDDLE AGED; MUTATION; PEDIGREE; PRESCHOOL CHILD;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; APOLIPOPROTEINS B; CHILD; CHILD, PRESCHOOL; FEMALE; HETEROZYGOTE; HOMOZYGOTE; HUMANS; HYPOBETALIPOPROTEINEMIAS; MALE; MIDDLE AGED; MUTATION; PEDIGREE;

EID: 1542651812     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9163     Document Type: Article

References (0)