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Lapicka-Bodzioch, Katarzyna ; Bodzioch, Marek ; Krüll, Matthias ; Kielar, Danuta ; Probst, Mario ; Kiec, Beata ; Andrikovics, Hajnalka ; Böttcher, Alfred ; Hubacek, Jaroslav ; Aslanidis, Charalampos ; Suttorp, Norbert ; Schmitz, Gerd

Homogeneous assay based on 52 primer sets to scan for mutations of the ABCA1 gene and its application in genetic analysis of a new patient with familial high-density lipoprotein deficiency syndrome

Lapicka-Bodzioch, Katarzyna, Bodzioch, Marek, Krüll, Matthias, Kielar, Danuta, Probst, Mario, Kiec, Beata, Andrikovics, Hajnalka, Böttcher, Alfred, Hubacek, Jaroslav, Aslanidis, Charalampos, Suttorp, Norbert and Schmitz, Gerd (2001) Homogeneous assay based on 52 primer sets to scan for mutations of the ABCA1 gene and its application in genetic analysis of a new patient with familial high-density lipoprotein deficiency syndrome. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 1537 (1), pp. 42-48.

Date of publication of this fulltext: 19 Dec 2024 15:50
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Item typeArticle
Journal or Publication TitleBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
Publisher:ELSEVIER SCIENCE BV
Place of Publication:AMSTERDAM
Volume:1537
Number of Issue or Book Chapter:1
Page Range:pp. 42-48
Date2001
InstitutionsMedicine > Lehrstuhl für Klinische Chemie und Laboratoriumsmedizin
Identification Number
ValueType
10.1016/S0925-4439(01)00053-9DOI
KeywordsBINDING CASSETTE TRANSPORTER-1; TANGIER-DISEASE; CHOLESTEROL; ABCA1; familial high-density lipoprotein deficiency; Tangier disease; genetic testing
Dewey Decimal Classification600 Technology > 610 Medical sciences Medicine
StatusPublished
RefereedYes, this version has been refereed
Created at the University of RegensburgYes
Item ID73539

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