Title : Phenotypic expression of familial hypobetalipoproteinemia in three kindreds with mutations of apolipoprotein B gene.

Pub. Date : 2001 Oct

PMID : 11590210






1 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 kindred, the proband is heterozygous for a T-deletion in exon 26, which converts tyrosine at codon 3435 into a stop codon, resulting in apoB-75.7. Tyrosine apolipoprotein B Homo sapiens