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Mutation analysis in a small cohort of New Zealand patients originating from the United Kingdom demonstrates genetic heterogeneity in familial hypercholesterolemia.
Thiart, R; Varret, M; Lintott, C J; Scott, R S; Loubser, O; du Plessis, L; de Villiers, J N; Boileau, C; Kotze, M J.
Affiliation
  • Thiart R; MRC Cape Heart Group, Tygerberg, South Africa. rthiart@gerga.sun.ac.za
Mol Cell Probes ; 14(5): 299-304, 2000 Oct.
Article in En | MEDLINE | ID: mdl-11040093
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Collection: 01-internacional Database: MEDLINE Main subject: Apolipoproteins B / Receptors, LDL / DNA Mutational Analysis / Hyperlipoproteinemia Type II Limits: Adult / Aged / Female / Humans / Male / Middle aged Country/Region as subject: Europa / Oceania Language: En Journal: Mol Cell Probes Journal subject: BIOLOGIA MOLECULAR / BIOTECNOLOGIA Year: 2000 Document type: Article Affiliation country: Country of publication:
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Apolipoproteins B / Receptors, LDL / DNA Mutational Analysis / Hyperlipoproteinemia Type II Limits: Adult / Aged / Female / Humans / Male / Middle aged Country/Region as subject: Europa / Oceania Language: En Journal: Mol Cell Probes Journal subject: BIOLOGIA MOLECULAR / BIOTECNOLOGIA Year: 2000 Document type: Article Affiliation country: Country of publication: