MOLECULAR GENETICS OF FAMILIAL HYPOBETALIPOPROTEINEMIA. GENETIC HETOROGENEITY AND CLINICAL IMPACT OF THE DISEASE
- 2 Anni 1999/2001
- 82.633€ Totale Fondi
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Pubblicazioni Scientifiche
- BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
Hypobetalipoproteinemia with an apparently recessive inheritance due to a "de novo" mutation of apolipoprotein B
- JOURNAL OF HEPATOLOGY
A study of fatty liver disease and plasma lipoproteins in a kindred with familial hypobetalipoproteinemia due to a novel truncated form of apolipoprotein B (APO B-54.5)
- JOURNAL OF LIPID RESEARCH
Phenotypic expression of familial hypobetalipoproteinemia in three kindreds with mutations of apolipoprotein B gene
