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Article

Identification of a nonsense mutation in the very low-density lipoprotein receptor gene (VLDLR) in an Iranian family with dysequilibrium syndrome

28 Nov 2007

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 18043714
DOI: 10.1038/sj.ejhg.5201967

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Identification of a nonsense mutation in the very low-density lipoprotein receptor gene (VLDLR) in an Iranian family with dysequilibrium syndromePMID 18043714Read ↗

Possible common mutations in the low density lipoprotein receptor gene in Chinese.Semantic proximity Read ↗

Novel VLDLR microdeletion identified in two Turkish siblings with pachygyria and pontocerebellar atrophySemantic proximity Read ↗

Mutations in <i>VLDLR</i> as a Cause for Autosomal Recessive Cerebellar Ataxia With Mental Retardation (Dysequilibrium Syndrome)Semantic proximity Read ↗

A missense founder mutation in VLDLR is associated with Dysequilibrium Syndrome without quadrupedal locomotion.Semantic proximity Read ↗

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A novel mutation of apolipoprotein B in a French Canadian family with homozygous hypobetalipoproteinemia.Semantic proximity Read ↗

Cerebellar ataxia, mental retardation and dysequilibrium syndrome 1 (CAMRQ1) caused by an unusual constellation of VLDLR mutation.Semantic proximity Read ↗

Detection of the apoB-3500 mutation in a Russian family with coronary heart disease.Semantic proximity Read ↗

Two novel and two known low-density lipoprotein receptor gene mutations in German patients with familial hypercholesterolemia.Semantic proximity Read ↗

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